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Intervention to End Recurrent Unscheduled Bleeding Trial

Intervention to End Recurrent Unscheduled Bleeding Trial: A Randomized-controlled Trial of Ulipristal Acetate for Unscheduled Bleeding in Etonogestrel Implant Users

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03118297
Acronym
INTERRUPT
Enrollment
65
Registered
2017-04-18
Start date
2017-05-01
Completion date
2018-01-31
Last updated
2018-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bleeding, Contraception

Keywords

Etonogestrel Implant

Brief summary

The subdermal etonogestrel (ENG) implant, a long-acting reversible contraceptive (LARC) method, is among the most effective forms of reversible contraception and thus, an important tool in the quest to reduce unintended pregnancy. However, despite overall increases in LARC use in the United States from 1.5% in 2002 to 7.2% in 2011, and 11.6% most recently in 2015, implant use continues to make up a small proportion of LARC use. While evidence to explain this low uptake of implants is lacking, one potential reason is patient and provider concerns about unpredictable bleeding. As a result of this, many studies have been performed in attempts to discover therapies for unscheduled bleeding in progestin-only contraceptive users. Some of these studies include those investigating selective progesterone receptor modulators, such as mifepristone and ulipristal acetate (UPA), which did find some benefit. Although a previous study showed mixed benefit, the investigators feel that this medication has demonstrated both biologic plausibility as well as clinically important outcomes. This previous study may not be entirely translatable to the proposed research as therapies were used for different indications (prophylaxis vs. treatment) and different progestins and delivery systems were studied. Therefore, the investigators believe UPA should not be discounted as a potential therapy. UPA may provide an additional safe and effective option for treatment of irregular bleeding with implants in women. In addition, UPA is currently available in outpatient pharmacies in the U.S. as a single 30mg oral tablet. The investigators propose to investigate UPA for the treatment of unscheduled and troublesome bleeding in ENG implant users.

Detailed description

The subdermal etonogestrel (ENG) implant, a long-acting reversible contraceptive (LARC) method, is among the most effective forms of reversible contraception and thus, an important tool in the quest to reduce unintended pregnancy. Despite this, ENG implant users make up a small percent of overall women that use LARC in the United States. Previous studies have demonstrated that among women dissatisfied with their implant, the majority cite unpredictable and irregular bleeding as a primary reason. Dissatisfaction with a contraceptive method can lead to discontinuation, which can put a woman at risk for unplanned pregnancy. Although irregular bleeding is a common side effect of all progestin-only contraceptives, there are significant gaps in our knowledge regarding the etiology of and effective therapies for unscheduled bleeding. While several mechanisms have been proposed and therapies have been studied, lack of convincing scientific evidence, in addition to possible contraindications to these therapies, demonstrates the need to investigate additional effective interventions. Studies evaluating interventions for abnormal uterine bleeding resulting from uterine leiomyoma provide insight into potential therapies for progestin-mediated bleeding. In prior studies, ulipristal acetate (UPA) has been shown to reduce bleeding symptoms associated with uterine leiomyoma, including decreasing or stopping excessive bleeding. Progestin-associated irregular bleeding has been proposed to be secondary to a disruption in endometrial angiogenesis, therefore creating a fragile venous network. UPA may displace local progestin to counteract this effect. Thus, this medication has demonstrated both biologic plausibility as well as clinically important benefits. UPA may provide an additional safe and effective option for treatment of irregular bleeding in implant users. As women are often dissatisfied with irregular bleeding with the implant as noted above, improving bleeding profiles could potentially improve uptake and continuation of the device. The investigators will perform a double blinded, randomized, placebo-controlled trial. Women will be randomized to receive either 15mg of UPA daily for 7 days or placebo for the same duration. The investigators hypothesize that UPA will decrease bleeding and spotting days in users of the ENG implant with unscheduled bleeding when compared to placebo as assessed by daily bleeding diaries.

Interventions

DRUGPlacebo oral capsule

Women who have bothersome bleeding with the etonogestrel implant will be randomized to receive ulipristal acetate versus placebo daily for 7 days.

DRUGUlipristal Acetate

Women who have bothersome bleeding with the etonogestrel implant will be randomized to receive ulipristal acetate versus placebo daily for 7 days.

Sponsors

Washington University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Women age 18-45 * Implant placed \>90 days and \<3 years prior to enrollment * Patient complaint of bothersome irregular bleeding with implant * Willing to be abstinent or use condoms during study period * Willing to complete 30-day bleeding diary * Willing to be randomized to placebo or ulipristal acetate * Ability to send/receive SMS text message

Exclusion criteria

* Non-English speaking * Implant placed \>3 years prior to enrollment * Contraindication to ulipristal acetate (current use of barbiturates, bosentan, carbamazepine, felbamate, griseofulvin, oxcarbazepine, phenytoin, rifampin, St. John's Wort, topiramate, known or suspected pregnancy, hypersensitivity to active substance or excipients, uterine/cervical/ovarian/breast cancer, severe asthma insufficiently controlled by oral glucocorticoids) * Inability or unwillingness to comply with medication protocol * Inability or unwillingness to comply with bleeding diary * Breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Number of Bleeding/Spotting Days With Use of Ulipristal Acetate as Measured by Daily Bleeding Diaries30 daysTo evaluate the effectiveness of ulipristal acetate (15mg) in decreasing bleeding/spotting days due to the ENG implant over a 30-day period as compared to placebo.

Secondary

MeasureTime frameDescription
Number of Participants With Bleeding Cessation by Day 1010 daysTo evaluate bleeding cessation rates by day 10 following seven days of treatment with either ulipristal acetate or placebo.
Participant Satisfaction With Bleeding Pattern at 30 Days30 daysTo evaluate participant satisfaction with regards to bleeding pattern after use of ulipristal acetate.
Number of Participants With Medication Side Effects by 30 Days30 daysTo evaluate participant satisfaction with regards to medication side effects.
Ovulation Status Measured by Weekly Serum Progesterone LevelsBaseline, weeks 1, 2, 3, 4To evaluate effect, if any, of ulipristal acetate on ovulation status. Data in the table represent the lowest and highest values that were recorded over all of the measurements for each arm as a whole.

Countries

United States

Participant flow

Participants by arm

ArmCount
Ulipristal Acetate
15mg ulipristal acetate (capsule) daily for 7 days Ulipristal Acetate: Women who have bothersome bleeding with the etonogestrel implant will be randomized to receive ulipristal acetate versus placebo daily for 7 days.
32
Placebo
Identical placebo (capsule) daily for 7 days Placebo oral capsule: Women who have bothersome bleeding with the etonogestrel implant will be randomized to receive ulipristal acetate versus placebo daily for 7 days.
33
Total65

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up02

Baseline characteristics

CharacteristicPlaceboTotalUlipristal Acetate
Age, Continuous25.5 years
STANDARD_DEVIATION 6.3
26.0 years
STANDARD_DEVIATION 6.2
26.4 years
STANDARD_DEVIATION 6.2
BMI27.8 kg/m^2
STANDARD_DEVIATION 7
28.7 kg/m^2
STANDARD_DEVIATION 7.6
29.6 kg/m^2
STANDARD_DEVIATION 8.2
Days of bleeding in 30 days prior to enrollment20.0 days20.3 days20.5 days
Duration of implant use9.2 months10.1 months10.9 months
Ethnicity (NIH/OMB)
Hispanic or Latino
2 Participants2 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
29 Participants61 Participants32 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Race
Black
21 Participants41 Participants20 Participants
Race/Ethnicity, Customized
Race
Other or multiracial
3 Participants8 Participants5 Participants
Race/Ethnicity, Customized
Race
White
7 Participants14 Participants7 Participants
Region of Enrollment
United States
31 participants63 participants32 participants
Sex: Female, Male
Female
31 Participants63 Participants32 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 320 / 33
other
Total, other adverse events
0 / 320 / 33
serious
Total, serious adverse events
0 / 320 / 33

Outcome results

Primary

Number of Bleeding/Spotting Days With Use of Ulipristal Acetate as Measured by Daily Bleeding Diaries

To evaluate the effectiveness of ulipristal acetate (15mg) in decreasing bleeding/spotting days due to the ENG implant over a 30-day period as compared to placebo.

Time frame: 30 days

Population: See baseline characteristics

ArmMeasureValue (MEDIAN)
Ulipristal AcetateNumber of Bleeding/Spotting Days With Use of Ulipristal Acetate as Measured by Daily Bleeding Diaries7 days
PlaceboNumber of Bleeding/Spotting Days With Use of Ulipristal Acetate as Measured by Daily Bleeding Diaries12 days
p-value: 0.002Wilcoxon (Mann-Whitney)
Secondary

Number of Participants With Bleeding Cessation by Day 10

To evaluate bleeding cessation rates by day 10 following seven days of treatment with either ulipristal acetate or placebo.

Time frame: 10 days

Population: See baseline characteristics

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Ulipristal AcetateNumber of Participants With Bleeding Cessation by Day 1011 Participants
PlaceboNumber of Participants With Bleeding Cessation by Day 103 Participants
p-value: 0.032Fisher Exact
Secondary

Number of Participants With Medication Side Effects by 30 Days

To evaluate participant satisfaction with regards to medication side effects.

Time frame: 30 days

Population: See baseline characteristics

ArmMeasureGroupValue (NUMBER)
Ulipristal AcetateNumber of Participants With Medication Side Effects by 30 DaysFeeling flushed0 participants
Ulipristal AcetateNumber of Participants With Medication Side Effects by 30 DaysDizziness1 participants
Ulipristal AcetateNumber of Participants With Medication Side Effects by 30 DaysNausea/Vomiting1 participants
Ulipristal AcetateNumber of Participants With Medication Side Effects by 30 DaysOther1 participants
Ulipristal AcetateNumber of Participants With Medication Side Effects by 30 DaysAbdominal pain2 participants
Ulipristal AcetateNumber of Participants With Medication Side Effects by 30 DaysDid not experience26 participants
Ulipristal AcetateNumber of Participants With Medication Side Effects by 30 DaysHeadache3 participants
PlaceboNumber of Participants With Medication Side Effects by 30 DaysDid not experience23 participants
PlaceboNumber of Participants With Medication Side Effects by 30 DaysHeadache6 participants
PlaceboNumber of Participants With Medication Side Effects by 30 DaysNausea/Vomiting3 participants
PlaceboNumber of Participants With Medication Side Effects by 30 DaysFeeling flushed1 participants
PlaceboNumber of Participants With Medication Side Effects by 30 DaysAbdominal pain2 participants
PlaceboNumber of Participants With Medication Side Effects by 30 DaysDizziness1 participants
PlaceboNumber of Participants With Medication Side Effects by 30 DaysOther1 participants
p-value: >0.05Chi-squared
Secondary

Ovulation Status Measured by Weekly Serum Progesterone Levels

To evaluate effect, if any, of ulipristal acetate on ovulation status. Data in the table represent the lowest and highest values that were recorded over all of the measurements for each arm as a whole.

Time frame: Baseline, weeks 1, 2, 3, 4

Population: See baseline characteristics

ArmMeasureGroupValue (NUMBER)
Ulipristal AcetateOvulation Status Measured by Weekly Serum Progesterone LevelsLower endpoint0.0 ng/mL
Ulipristal AcetateOvulation Status Measured by Weekly Serum Progesterone LevelsUpper endpoint4.4 ng/mL
PlaceboOvulation Status Measured by Weekly Serum Progesterone LevelsLower endpoint0.0 ng/mL
PlaceboOvulation Status Measured by Weekly Serum Progesterone LevelsUpper endpoint1.3 ng/mL
Secondary

Participant Satisfaction With Bleeding Pattern at 30 Days

To evaluate participant satisfaction with regards to bleeding pattern after use of ulipristal acetate.

Time frame: 30 days

Population: See baseline characteristics

ArmMeasureCategoryValue (COUNT_OF_PARTICIPANTS)
Ulipristal AcetateParticipant Satisfaction With Bleeding Pattern at 30 DaysNot at all happy0 Participants
Ulipristal AcetateParticipant Satisfaction With Bleeding Pattern at 30 DaysSomewhat unhappy0 Participants
Ulipristal AcetateParticipant Satisfaction With Bleeding Pattern at 30 DaysNeither happy nor unhappy4 Participants
Ulipristal AcetateParticipant Satisfaction With Bleeding Pattern at 30 DaysSomewhat happy5 Participants
Ulipristal AcetateParticipant Satisfaction With Bleeding Pattern at 30 DaysVery happy23 Participants
Ulipristal AcetateParticipant Satisfaction With Bleeding Pattern at 30 DaysDid not respond0 Participants
PlaceboParticipant Satisfaction With Bleeding Pattern at 30 DaysVery happy8 Participants
PlaceboParticipant Satisfaction With Bleeding Pattern at 30 DaysNot at all happy7 Participants
PlaceboParticipant Satisfaction With Bleeding Pattern at 30 DaysSomewhat happy10 Participants
PlaceboParticipant Satisfaction With Bleeding Pattern at 30 DaysSomewhat unhappy2 Participants
PlaceboParticipant Satisfaction With Bleeding Pattern at 30 DaysDid not respond1 Participants
PlaceboParticipant Satisfaction With Bleeding Pattern at 30 DaysNeither happy nor unhappy3 Participants
p-value: <0.001Fisher Exact

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026