A randomized single-blind non-inferiority trial of delayed start with drospirenone-only and ethinyl estradiol-gestodene pills for ovulation inhibition

We compared the efficacy of 4 mg drospirenone (DRSP) progestin-only pills (POPs) versus combined oral contraceptive pills (COCs) containing 0.02 mg of ethinyl estradiol (EE) and 0.075 mg of gestodene (GS) in ovulation inhibition and inducing unfavorable cervical mucus changes using a delayed-starting approach. This randomized controlled trial involved 36 participants aged 18–45 years. The major outcomes included ovulation inhibition assessed using the Hoogland and Skouby score, and cervical mucus permeability, assessed using the modified World Health Organization score. The results demonstrated ovulation inhibition rates of 77.8% for the EE/GS group and 88.9% for the DRSP group. The risk ratio and absolute risk reduction were 0.50 (95% confidence interval [CI]: 0.10, 2.40) and − 0.11 (95% CI: − 0.35, 0.13), respectively, satisfying the 20% non-inferiority margin threshold. The median time to achieve unfavorable cervical mucus changes was comparable between the DRSP (3 days, interquartile range [IQR]: 6 days) and EE/GS (3.5 days, IQR: 4 days) groups. However, the DRSP group had a higher incidence of unscheduled vaginal bleeding (55.56% vs. 11.11%; p = 0.005). DRSP-only pills, initiated on days 7–9 of the menstrual cycle, were non-inferior to EE/GS pills in ovulation inhibition. However, they exhibited delayed unfavorable cervical mucus changes compared to the standard two-day backup recommendation. Clinical trial registration: Thai Clinical Trials Registry (TCTR20220819001) https://www.thaiclinicaltrials.org/show/TCTR20220819001.

conditions, whereas the contraindications to POPs are limited 9 .Newer POPs containing 4 mg of drospirenone (DRSP) have shown superior ovulation inhibition (96.3%) than desogestrel-based POPs, but are contraindicated in individuals with renal insufficiency or untreated hyperaldosteronism 11 .DRSP-based POPs showed a low overall ovulation rate (0.9%) despite multiple intentional 24-h delays in pill intake, representing the same safety window of delayed intake as COCs 12 .
Access to contraception can be delayed if a woman needs to wait to initiate the OCPs at the beginning of the menstrual cycle.Quick-starting contraception, which is initiated immediately at the woman's request, may lead to fewer unintended pregnancies due to increased access, convenience, and better adherence and continuation [13][14][15] .International guidelines recommend quick-starting with backup contraception 9,[16][17][18][19] .In this approach, while 7 days of additional contraception are recommended for COCs based on their mechanism of ovulation inhibition, only 2 days of additional contraception with POPs are recommended considering cervical mucus blockage, the primary mechanism of action of traditional POPs 9,16 .Despite these recommendations, few clinical studies have demonstrated the efficacy of OCPs in delayed-starting cycles, particularly for ovulation inhibition and follicular activity 15,[20][21][22][23][24][25][26] .
We compared 4 mg DRSP-only pills with ultra-low-dose COCs for ovulation inhibition, starting treatment on days 7-9 of the menstrual cycle.This timing reflects common delays in real-world contraceptive use, and the choice of ultra-low-dose COCs aligns with current trends in reducing hormone levels while maintaining effectiveness, and is supported by recent studies on delayed COCs initiation 20,21,27,28 .We set a 20% non-inferiority margin in ovulation inhibition compared to the active control, based on existing evidence 20 .Additionally, we evaluated the onset of changes in cervical mucus permeability, crucial for POPs recommendations.

Study design
We conducted a single-blinded (investigator-blinded), parallel-group, randomized, controlled, non-inferiority trial.The protocol was registered in the Thai Clinical Trials Registry (TCTR) and approved on August 19, 2022 (TCTR20220819001).The research protocol was designed in accordance with the International Good Clinical Practice regulations and the Declaration of Helsinki and was approved by the Institutional Review Board (IRB) of the Faculty of Medicine, Chulalongkorn University (0243/65).All participants provided written informed consent before enrollment, and received 500 bath (approximately $15) for each visit as compensation for the time spent on the project.
Randomization was performed using a computer-generated sequence by a biostatistician who was not involved in data analysis.The allocation ratio between the experimental treatment and active control was 1:1 with a block of four randomizations.Participants were assigned to groups using individually sealed envelopes, which were opened by a research assistant not involved in data analysis.Medication for each patient was provided in unique envelopes.To ensure investigator blinding in a single-blind study, participants were instructed to keep the medication in these envelopes during clinic visits.The primary investigator (RA), who was blinded to the study allocation and participants' hormone levels, performed transvaginal ultrasonography (TVUS) and cervical mucus evaluations.The investigators involved in data analysis (RA, US, PP, and SS) were blinded to the study intervention.

Participants
The participants were recruited from the Family Planning and Reproductive Health Unit of King Chulalongkorn Memorial Hospital (KCMH), Thailand and Internet advertisements 29,30 .We included women aged 18-45 years (body mass index [BMI], 18-30 kg/m 2 ) with a history of regular menstrual cycles of 24-38 days.The exclusion criteria were contraindications to estrogen or progestin therapy 9 , pregnancy or lactation, exogenous hormone use (estrogen, progestin, or testosterone) in the past 3 months, or the presence of precancerous or cancerous cervical lesions, ovarian cysts, suspected ovarian tumors, or a pre-existing dominant follicle larger than 10 mm on the initial screening TVUS, which is crucial for accurately determining the participant's menstrual date.

Study protocol
The initial screening was conducted on the first or second day of the menstrual cycle (visit 0), during which a complete medical history, general physical examination, and TVUS were performed.Unless male or female sterilization was used for contraception, the participants were instructed to use male condoms during the study period.
The first visit after enrollment (visit 1, also referred to as the starting medication day) was timed to occur on days 7-9 of the menstrual cycle.During this visit, TVUS was used to assess ovarian activity, cervical mucus was collected, and blood was drawn for the measurement of serum estradiol, progesterone, and LH levels.At this visit, participants were randomized into two groups, receiving either DRSP or EE/gestodene (GS), and were provided with their respective medications and a menstrual diary for recording.
Follow-up visits were initially scheduled every 2-3 days to monitor for signs of ovulation inhibition, evaluate cervical mucus quality, and measure serum levels of estradiol, progesterone, and LH.These visits continued at this frequency until ovulation was observed or until cervical mucus assessments yielded a modified WHO score of ≤ 4 or the largest follicle diameter (LFD) was < 13 mm on two consecutive occasions, indicating unfavorable fertility conditions 31 .Following these outcomes, the frequency of the follow-up visits was adjusted to a weekly basis, allowing for continued assessments via TVUS until the completion of the 28-day medication course.

Outcomes
The primary outcome was ovulation inhibition, as defined by the Hoogland and Skouby score, as shown in Fig. S1 20,33 .Secondary outcomes were the time required to achieve unfavorable mucus after treatment initiation and adverse events.Follicle like structures refers to the follicles or cystic ovarian structures observed on TVUS, which were measured by averaging the two largest perpendicular diameters in millimeters (mm).TVUS was performed using a Phillips Affiniti 70G (SN: US919F1869) with a transvaginal probe (C10-3V; 10-3 MHz).
Morning blood samples were collected in 5-mL clot-activated tubes and sent within 30 min to the laboratory center, Faculty of Medicine, Chulalongkorn University, ISO 15189.An electrochemiluminescence immunoassay (ECLIA, Cobas, Switzerland) was used to measure serum estradiol and progesterone levels using the competition method and to measure serum LH using the sandwich method.The intra-and inter-assay coefficients of variation were less than 4%.The minimum detection limits were 18.35 pmol/L for estradiol, 0.159 nmol/L for progesterone, and 0.1 IU/L for LH.Our study used the standard progesterone level of 5 nmol/L or 1.57 ng/mL, as defined by the Hoogland and Skouby score, to indicate ovulation 33 .

Follicular dynamics
After completing the treatment cycle, follicular dynamics were sorted into four categories based on the Hoogland and Skouby score, as shown in Fig. S2 20 .

Cervical mucus assessment
Cotton swabs were used to wipe the external cervical os.A syringe was then inserted 1-2 cm into the cervical canal, and gentle suction was applied to aspirate the mucus.Within 30 min, a trained scientist (WR) assessed the mucus using the methodology in WHO Laboratory Manual 5th Edition, as shown in Fig. S3 31 .Each parameter was photographed, recorded, and confirmed by the principal investigator (RA).Inconclusive results were discussed by the RA and WR.
We used a modified WHO scoring system with a maximum score of 12, and defined scores ≤ 4 as indicating unfavorable mucus, as shown in Fig. S4 31 .Since progesterone reduces mucus permeability, cycles in which ovulation occurred before the cervical mucus became unfavorable were excluded from the analysis.

Bothersome adverse events
Participants recorded the adverse events in their diaries.Unscheduled bleeding was defined by evidence of blood loss that requires the use of sanitary protection with a tampon, pad or pantyliner during active tablet ingestion 32 .The diary logs were evaluated at each follow-up appointment.

Sample size
Duijkers et al. stated that 4 mg of DRSP taken on day 1-2 of menstruation is highly effective in inhibiting ovulation, even with a 24-h delay protocol 11,12 .Jirakittidul et al. reported that ultra-low dose COCs containing EE/GS had a 95.6% ovulation-inhibition rate in the delayed-starting approach 20 .We aimed to determine if DRSP 4 mg inhibited ovulation comparable to that of EE/GS.Our study used a non-inferiority design with 80% power, a 1-sided test alpha of 5%, and a non-inferiority margin of 20%.The final sample size was 18 per group, accounting for a 30% dropout rate.

Statistical analysis
Research Electronic Data Capture (REDCap), administered by Chulalongkorn University, was used to collect and manage the data 34 .STATA version 17 (StataCorp.2021.Stata Statistical Software: Release 17. College Station, TX: StataCorp LLC.) was used for analyses.Descriptive statistics were used as appropriate.To evaluate the intergroup differences in the ovulation-inhibition, we used univariable logistic regression and presented the results as risk ratios (RRs) and 95% confidence intervals (CIs).We calculated the absolute risk difference (ADR) and 95% CI to show that our results were within the 20% non-inferiority margin.The multivariable analyses were adjusted for age.The cumulative incidence of ovulation was analyzed using the Kaplan-Meier survival estimation and the log-rank test for survival function equality.Statistical significance was set at p < 0.05.We conducted both per protocol (PP) and intention-to-treat (ITT) analyses but only reported the ITT results if both revealed comparable results.If there were differences, both results would be reported.For the ITT analysis, we imputed data using worst-case scenarios for most outcomes, including ovulation, follicular dynamics, and cervical mucus permeability.We imputed the data on the mean LFD, estradiol, and LH levels throughout the treatment cycle using the mean variable of that study group.

Results
Between August and December 2022, thirty-six participants were randomized to the control group (EE/GS) or study group (DRSP), as shown in Fig. 1.One participant from each group left the study because of scheduling conflicts; both were randomized, but neither took the study medication.One participant of the EE/GS group took the pill for 4 days and requested withdrawal from the study after experiencing adverse effects.No protocol deviations were observed.Finally, the PP analysis included 16 and 17 participants from the EE/GS and DRSP groups, respectively, while the ITT analysis included all participants.
The two study groups had comparable demographic characteristics (Table 1).The BMI distribution according to WHO and Center for Disease Control and Prevention (CDC) criteria showed that 5.56% and 11.11% of the participants in the EE/GS and DRSP groups, respectively, were clinically obese (BMI ≥ 27.5 and ≥ 30 kg/ m 2 , respectively) 35,36 .The proportions of participants who began taking the study medication on days 7, 8, and 9 of the menstruation cycle and the Hoogland scores of 1, 2, and 4, respectively, were comparable between the www.nature.com/scientificreports/groups (Table 2).LFD on the starting medication day did not differ significantly between the two groups, as shown in Table S1.
In both EE/GS and DRSP groups, ultrasound findings indicated suspected follicular rupture in up to onethird of cases (35.71% in EE/GS and 25.0% in DRSP).Despite these findings, there was no significant increase in progesterone levels, which remained below 5 nmol/L (1.57ng/mL) during at least two visits (spanning approximately 4-6 days) following the suspected follicular rupture in these participants.Ovulation inhibition, defined by follicular dynamics based on the Hoogland and Skouby score 33 , occurred in four (77.8%) and two (88.9%)patients in the EE/GS and DRSP groups, respectively (RR = 0.50, 95% CI: 0.104, 2.395, p = 0.386; Table 3).The absolute risk difference was − 0.110 (95% CI: − 0.352, 0.130), of which the 20% non-inferiority margin was 0.2 (Fig. 2).The multivariable analysis adjusted for age showed comparable results.In Fig. 3, we present the PP analysis of LFD, hormone levels, and ovulation dates of the three participants who ovulated.Two participants in the EE/GS group ovulated 3 days after beginning the study medication, whereas one participant in the DRSP group ovulated 7 days after starting the medication.Figure 4 illustrates the LFD, estrogen, and LH levels throughout the study period.As the cycles progressed, LFD tended to decrease in the EE/GS group, while the serum estrogen levels tended to be lower in the DRSP group.The LH levels were comparable between the two groups.During the study, 36 participants were observed for 861 person-days and three instances of ovulation occurred, as determined by the PP analysis.The Kaplan-Meier curve showed an incidence of 3.48 per 1000 person-days (95% CI: 1.12-10.80),with no significant difference between the two groups (p = 0.499), as shown in Fig. 5. Table 3 presents the Hoogland and Skouby scores at the end of the treatment cycle, in which approximately half of the participants in the EE/GS group showed no ovarian activity.
The mean duration for achieving the modified WHO cervical mucus score ≤ 4 after taking the medication is shown in Table 3.It took a median time (IQR) of 3.50 (4) in the EE/GS and 3 (6) days in the DRSP group to achieve unfavorable cervical mucus change.Within 7 days, cervical mucus changes were observed in nearly all participants, with one exception from each group.In the DRSP group, one participant did not experience cervical mucus changes.In contrast, the exception in the EE/GS group experienced these changes on 10 days after starting the study medication.
The incidence of unscheduled bleeding was significantly higher in the DRSP group (55.56%) than in the EE/ GS group (10%; p = 0.005), as shown in Table 4.One participant in the EE/GS group discontinued the study due to palpitation after 4 days of medicine administration, when physical examination and electrocardiogram showed normal findings and normal sinus rhythm, respectively.Other adverse events were comparable between the groups (Table 4).The blood pressure and weight measurements obtained before and after medication administration are shown in Table S2.

Main findings
This study established a 20% non-inferiority margin of ovulation inhibition between ultra-low dose COCs (EE/ GS) and POPs containing 4 mg of DRSP in a delayed-starting regimen on days 7-9 of the menstrual cycle, of which ovulation inhibition was demonstrated in 77.8% and 88.9% of participants, respectively.Most participants experienced unfavorable cervical mucus changes within the first 7 days, which exceeded the standard two-day backup recommendation 16 .
Jirakittidul et al. 's study on a delayed-starting regimen of ultralow-dose COCs (EE/GS) in a design with a fixed-cycle day 20 revealed that the ovulation-inhibition rate was 95.6% when medication was started on days 7-9 of the menstrual cycle.However, while majority of our participants started the intervention on days 8-9, representing only half of those with no demonstrated ovarian activity, the corresponding proportion in the study by Jirakittidul et al. was approximately 75% 20 .This may explain the differences in the ovulation rates in the two studies.
Several studies have reported discrepancies between ultrasound findings and serum progesterone levels when determining the Hoogland and Skouby score [37][38][39] .Therefore, our primary method for determining ovulation based on the Hoogland and Skouby scores relied on serum progesterone elevation.This discrepancy between the ultrasound findings and progesterone levels posed a challenge in establishing ovulation using the Hoogland and Skouby score.Other studies facing this challenge have defined ovulation based solely on progesterone levels when ultrasound findings were inconclusive and have used anovulation status as the outcome measure 37,39 .Additionally, measuring estradiol, which must exceed 200 pg/mL for at least 50 h to induce LH release preceding ovulation,  GS group started medication on day seven of menstruation when the LFD was 11.8 mm, the LH level was 15.72 IU/mL, and the estradiol level was 296.67 ng/mL.Ovulation was suspected on day three after the intervention, as TVUS showed the sudden disappearance of LFD.On day eight, progesterone level rose to 13.10 ng/mL.(B) Patient ID 32 in the EE/GS group started medication on day eight of menstruation when the LFD was 16.9 mm, the LH level was 4.94 IU/mL, and the estradiol level was 277.87 ng/mL.Ovulation was suspected on day three after the intervention, as TVUS showed collapsed LFD.On day seven, progesterone level rose to 5.36 ng/mL.(C) Patient ID 36 in the DRSP group started medication on day eight of menstruation when the LFD was 11.0 mm, the LH was 4.09 IU/mL, and the estradiol level was 69.87 ng/mL.On day five following intervention, LFD was 16.3 mm, the LH level was 19.9 IU/L, and the estradiol level was 305.64 ng/mL.Ovulation was suspected on day seven after the intervention, as TVUS showed collapsed LFD.On day 12, progesterone level rose to 16.71 ng/mL.EE/GS ethinyl estradiol 0.020 mg plus gestodene 0.075 mg, DRSP 4 mg drospirenone, Day 0 starting medication day, LFD leading follicle diameter, LH Luteinizing hormone, P4 Progesterone, E2 Estradiol, TVUS transvaginal ultrasound.could offer clearer ovulation detection 40 .However, this approach requires frequent testing, which was beyond the scope of this study but could be considered in future research for enhanced accuracy.
Among the discrepant findings for hormonal and follicular dynamics, one distinct pattern was an increase in LH levels, indicating an LH surge, followed by a decline to baseline levels, despite follicular rupture occurring over time.This pattern deviated from the normal cycle, wherein follicular rupture occurred 28-36 h after the onset of the LH surge 41 .Erden et al. 42 identified three physiological events occurring after the LH surge in the natural ovulatory cycle: resumption of first meiotic division at a low LH level; luteinization of granulosa cells at higher LH levels; and follicle wall rupture at very high LH levels 43 .Erden et al. concluded that the interval between the onset of the LH surge and ovulation typically ranged from 22 to 56 h in a normal ovulatory cycle 42,44 .Thus, the delayed follicular rupture following an LH surge without an increase in progesterone levels could be attributed to the contraceptive mechanism inducing an abnormal LH surge 43 .
A significant disparity was observed between the two groups, with approximately two-thirds of the participants in the EE/GS group showing no follicular growth or regression and only one-third of the participants in the DRSP group showing this pattern.This observation was further supported by the time trend of the LFD (Fig. 4).Participants in the DRSP group exhibited larger LFD values as the cycles progressed.Notably, a persistent follicle was the most distinctive characteristic of the DRSP group, with approximately half of the participants experiencing this phenomenon 45 .This finding can be attributed to the estrogen component of combined oral contraceptives (COC), which inhibits FSH secretion, suppressing follicle growth and reducing overall follicular activity 3,7,8 .Another explanation could be variations in progestin types, which may warrant further study.
Branche et al. studied the pharmacodynamics of delayed-starting desogestrel 0.075 mg, used after ulipristal acetate emergency contraception 46 .In one arm of their study, POPs were administered alone when the follicle reached 14-16 mm, which corresponds to the late follicular phase.An unfavorable cervical mucus was achieved in 76% (16/21) of the participants within 2 days of medicine administration and in all participants within 4 days.In contrast, our study administered the medicine when the LFD was approximately 10 mm.Within 10 days, all participants, except one in the DRSP group, exhibited a change to unfavorable cervical mucus.Our findings imply that 2 days may be insufficient for backup; however, given the limited scope and sample size of our study, we cannot definitively recommend extending the backup period for DRSP-based POPs.Additional research is needed to explore the timing of achieving cervical mucus change when using pills containing only DRSP, as this may differ from that in other POPs.
Han et al. 's review 47 criticized the lack of specific studies correlating changes in the cervical mucus score with the risk of pregnancy and highlighted that the recommendation regarding cervical mucus was based on expert opinions with limited clinical evidence.Additionally, the Sentinel study on cervical mucus did not assess the drug's impact on the periovulatory period, which shows the highest mucus production 10 .Most clinical guidelines over almost half a century have failed to reference the primary literature on the contraceptive effects of cervical secretions 9,[16][17][18][19] .

Strengths and limitations
The effectiveness of POPs for delayed-starting contraception has been evaluated in only a few studies 46 .Our study addressed this gap by evaluating the effectiveness of POPs using a Hoogland and Skouby score, the standard algorithm for assessing ovulation 33 .To ensure the validity and reliability of the results and to minimize bias, cervical mucus scoring was performed by a well-trained researcher blinded to the study intervention.Cervical mucus was evaluated according to the WHO Laboratory Manual 5th Edition methodology criteria 31 .We also implemented measures to monitor participants' adherence.We requested that all participants respond to a chat message regarding medicine ingestion, thereby minimizing protocol violations.
While daily monitoring yields the best assessment of ovulation outcomes, we mitigated this limitation by incorporating progesterone level assessments and serial ultrasound scans conducted by a single operator.Another limitation was that our protocol was designed to evaluate ovulation inhibition, which influenced the focus of our follow-up visits.Thus, the evaluation interval for cervical mucus was set at either 36 h or 60 h after medication administration, potentially affecting the timing of the cervical mucus change and its interpretation.While the randomization process yielded comparable baseline characteristics among the study participants, those in the DRSP group had a smaller LFD on the starting day of medication.Although the difference was small and did not reach statistical significance, it could still contribute to better ovulation suppression.Additionally, since our study was designed based on non-inferiority, we could not determine whether POPs were superior to COCs in terms of ovulation inhibition with a delayed-starting approach.Critically, the choice of a 20% non-inferiority margin, while consistent with prior studies 20,21 , was not derived from specific empirical evidence, which may limit the precision of our conclusions regarding the comparative effectiveness of the contraceptive methods studied.Considering the fixed-cycle study design in clinical practice, addressing the knowledge gap associated with subgroup evaluation based on menstrual cycle duration, particularly in women with short menstrual intervals, is crucial.Moreover, the challenges arising when POPs are administered in the late follicular phase also require consideration.

Conclusions
Our study demonstrated the non-inferiority of ovulation inhibition by 4-mg DRSP-only pills in comparison with COCs containing EE 0.02 mg and GS 0.075 mg in a delayed-starting approach when medication was administered on days 7-9 of the menstrual cycle.We found delayed unfavorable cervical mucus changes that exceeded the 2-day backup recommendation.

Figure 3 .
Figure 3. Follicular activity and hormonal levels among the three participants who ovulated.(A) Patient ID 30 in the EE/GS group started medication on day seven of menstruation when the LFD was 11.8 mm, the LH level was 15.72 IU/mL, and the estradiol level was 296.67 ng/mL.Ovulation was suspected on day three after the intervention, as TVUS showed the sudden disappearance of LFD.On day eight, progesterone level rose to 13.10 ng/mL.(B) Patient ID 32 in the EE/GS group started medication on day eight of menstruation when the LFD was 16.9 mm, the LH level was 4.94 IU/mL, and the estradiol level was 277.87 ng/mL.Ovulation was suspected on day three after the intervention, as TVUS showed collapsed LFD.On day seven, progesterone level rose to 5.36 ng/mL.(C) Patient ID 36 in the DRSP group started medication on day eight of menstruation when the LFD was 11.0 mm, the LH was 4.09 IU/mL, and the estradiol level was 69.87 ng/mL.On day five following intervention, LFD was 16.3 mm, the LH level was 19.9 IU/L, and the estradiol level was 305.64 ng/mL.Ovulation was suspected on day seven after the intervention, as TVUS showed collapsed LFD.On day 12, progesterone level rose to 16.71 ng/mL.EE/GS ethinyl estradiol 0.020 mg plus gestodene 0.075 mg, DRSP 4 mg drospirenone, Day 0 starting medication day, LFD leading follicle diameter, LH Luteinizing hormone, P4 Progesterone, E2 Estradiol, TVUS transvaginal ultrasound.

Table 1 .
Baseline characteristics.EE/GS ethinyl estradiol 0.02 mg plus gestodene 0.075 mg, DRSP 4 mg drospirenone, SD standard deviation, IQR interquartile range.a Student t-test, Wilcoxon rank-sum test, Chisquare or Fisher's exact tests as appropriate.b Backache and loss of appetite.

Table 2 .
Characteristic on the starting medication day.EE/GS ethinyl estradiol 0.02 mg plus gestodene 0.075 mg, DRSP 4 mg drospirenone, SD standard deviation, IQR interquartile range, FLS follicle like structure, LUF luteinized unruptured follicle.a Student t-test, Wilcoxon rank-sum test, Chi-square or fisher's exact tests as appropriate.

Table 4 .
Bothersome adverse events.EE/GS ethinyl estradiol 0.02 mg plus gestodene 0.075 mg, DRSP 4 mg drospirenone.a Chi-square or Fisher's exact tests as appropriate.b Number of participants experiencing unscheduled bleeding.c Duration of unscheduled bleeding in individuals experiencing this condition.d Mann-Whitney U test.