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NCT02314754 · ClinicalTrials.gov registry record · Phase 4
Outpatient Medical Abortion With Mifepristone and Misoprostol Through 77 Days of Gestation
A Phase 4 study, sponsored by Gynuity Health Projects.
- Completed
- Registry status
- Phase 4
- Development phase
- 719
- Enrollment target
NCT02314754: Completed Phase 4 study, sponsored by Gynuity Health Projects.
NCT02314754 is a Phase 4 study that has completed, run by Gynuity Health Projects. The registered enrollment target is 719 participants, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (39% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02314754, a Phase 4 study, has completed, sponsored by Gynuity Health Projects.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 719 participants
- Enrollment target
Study Summary
To demonstrate non-inferiority of the efficacy of 200 mg mifepristone followed in 24 to 48 hours by 800 µg buccal misoprostol in outpatient medical abortion services among women 71-77 days' compared to women 64-70 days' LMP.
Primary Outcome
Efficacy of medical abortion in the later first trimester as determined by the proportion of successful terminations without surgical intervention (suction curettage or D\&C) for any reason
Interventions
- DRUG Mifepristone followed by misoprostol 24-48 hours later
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 719 participants |
| Start Date | 2014-12 |
| Est. Completion | 2016-04 |
| Phase | Phase 4 |
What the finished NCT02314754 record still lists
NCT02314754 is an interventional study that assigns participants to a tested intervention. The registered 719 participants enrollment target is mid-sized for trials with a published cap, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (39% higher).
The record links to 0 conditions, and to 1 intervention - of which Mifepristone followed by misoprostol 24-48 hours later is the first listed.
NCT02314754 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02314754 about?
NCT02314754 is a clinical study titled "Outpatient Medical Abortion With Mifepristone and Misoprostol Through 77 Days of Gestation". To demonstrate non-inferiority of the efficacy of 200 mg mifepristone followed in 24 to 48 hours by 800 µg buccal misoprostol in outpatient medical abortion services among women 71-77 days' compared to women 64-70 days' LMP.
What is the current status of trial NCT02314754?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 719 participants. The study started on 2014-12. Estimated completion is 2016-04.
What interventions are being tested in trial NCT02314754?
The interventions under investigation include: Mifepristone followed by misoprostol 24-48 hours later (DRUG).
Who is sponsoring clinical trial NCT02314754?
This trial is sponsored by Gynuity Health Projects, which has 29 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02314754's enrollment target sits among peer trials
719 114th of 2000 higher than 1,887 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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