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NCT00835731 · ClinicalTrials.gov registry record · NA
Misoprostol Versus Dilapan-S for Cervical Preparation
A NA study, sponsored by Planned Parenthood League of Massachusetts.
- Completed
- Registry status
- NA
- Development phase
- 125
- Enrollment target
NCT00835731: Completed NA study, sponsored by Planned Parenthood League of Massachusetts.
NCT00835731 is a NA study that has completed, run by Planned Parenthood League of Massachusetts. The registered enrollment target is 125 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00835731, a NA study, has completed, sponsored by Planned Parenthood League of Massachusetts.
- COMPLETED
- Registry status
- NA
- Development phase
- 125 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the dilatory effect of 400 mcg of buccally administered misoprostol to one Dilapan-S rod placed 3-4 hours before abortion by dilation and evacuation in women who are 12 weeks 0 days to 15 weeks 0 days gestation.
Interventions
- DRUG misoprostol
- DEVICE Dilapan-S, vitamin B-12
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 125 participants |
| Start Date | 2009-01 |
| Est. Completion | 2011-12 |
| Phase | NA |
What the finished NCT00835731 record still lists
NCT00835731 is an interventional study that assigns participants to a tested intervention. The registered 125 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).
The record links to 0 conditions, and to 2 interventions - of which misoprostol is the first listed.
NCT00835731 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00835731 about?
NCT00835731 is a clinical study titled "Misoprostol Versus Dilapan-S for Cervical Preparation". The purpose of this study is to compare the dilatory effect of 400 mcg of buccally administered misoprostol to one Dilapan-S rod placed 3-4 hours before abortion by dilation and evacuation in women who are 12 weeks 0 days to 15 weeks 0 days gestation.
What is the current status of trial NCT00835731?
This trial is currently completed. It is a NA study. The enrollment target is 125 participants. The study started on 2009-01. Estimated completion is 2011-12.
What interventions are being tested in trial NCT00835731?
The interventions under investigation include: misoprostol (DRUG), Dilapan-S, vitamin B-12 (DEVICE).
Who is sponsoring clinical trial NCT00835731?
This trial is sponsored by Planned Parenthood League of Massachusetts, which has 13 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00835731's enrollment target sits among peer trials
125 753rd of 2000 higher than 1,243 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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