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NCT00386867 · ClinicalTrials.gov registry record · NA
A Randomized Trial of Buccal Compared to Oral Misoprostol Following Mifepristone for Medical Abortion up to 63 Days LMP
A NA study, sponsored by Gynuity Health Projects.
- Completed
- Registry status
- NA
- Development phase
- 1,200
- Enrollment target
NCT00386867: Completed NA study, sponsored by Gynuity Health Projects.
NCT00386867 is a NA study that has completed, run by Gynuity Health Projects. The registered enrollment target is 1,200 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (15% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00386867, a NA study, has completed, sponsored by Gynuity Health Projects.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,200 participants
- Enrollment target
Study Summary
This open-label, randomized study will compare the efficacy, safety, and acceptability of mifepristone 200 mg followed in 24-36 hours either by buccal (i.e., in the cheeks) or oral misoprostol 800 mcg for termination of pregnancy in women up to 63 days L.M.P.
Interventions
- DRUG 800 mcg misoprostol via oral or buccal administration
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,200 participants |
| Start Date | 2006-10 |
| Est. Completion | 2007-03 |
| Phase | NA |
What the finished NCT00386867 record still lists
NCT00386867 is an interventional study that assigns participants to a tested intervention. Its 1,200 participants enrollment target places it among the larger protocols in the corpus, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (15% lower).
The record links to 0 conditions, and to 1 intervention - of which 800 mcg misoprostol via oral or buccal administration is the first listed.
NCT00386867 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00386867 about?
NCT00386867 is a clinical study titled "A Randomized Trial of Buccal Compared to Oral Misoprostol Following Mifepristone for Medical Abortion up to 63 Days LMP". This open-label, randomized study will compare the efficacy, safety, and acceptability of mifepristone 200 mg followed in 24-36 hours either by buccal (i.e., in the cheeks) or oral misoprostol 800 mcg for termination of pregnancy in women up to 63 days L.M.P.
What is the current status of trial NCT00386867?
This trial is currently completed. It is a NA study. The enrollment target is 1,200 participants. The study started on 2006-10. Estimated completion is 2007-03.
What interventions are being tested in trial NCT00386867?
The interventions under investigation include: 800 mcg misoprostol via oral or buccal administration (DRUG).
Who is sponsoring clinical trial NCT00386867?
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 NCT00386867's enrollment target sits among peer trials
1,200 83rd of 2000 higher than 1,912 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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