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NCT00504465 · ClinicalTrials.gov registry record · NA
Combined Agent Randomized Trial of Induction of Labor
A NA study, sponsored by Weill Medical College of Cornell University.
- Completed
- Registry status
- NA
- Development phase
- 210
- Enrollment target
NCT00504465: Completed NA study, sponsored by Weill Medical College of Cornell University.
NCT00504465 is a NA study that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 210 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00504465, a NA study, has completed, sponsored by Weill Medical College of Cornell University.
- COMPLETED
- Registry status
- NA
- Development phase
- 210 participants
- Enrollment target
Study Summary
To compare sequential dinoprostone and oxytocin for induction of labor at term with intact membranes and an unripe cervix to two simultaneous regimens. Our aim was to confirm findings from smaller trials and add to data on fetal safety.
Interventions
- DRUG dinoprostone
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 210 participants |
| Start Date | 2002-05 |
| Est. Completion | 2007-04 |
| Phase | NA |
What the finished NCT00504465 record still lists
NCT00504465 is an interventional study that assigns participants to a tested intervention. The registered 210 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 (85% lower).
The record links to 0 conditions, and to 1 intervention - of which dinoprostone is the first listed.
NCT00504465 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00504465 about?
NCT00504465 is a clinical study titled "Combined Agent Randomized Trial of Induction of Labor". To compare sequential dinoprostone and oxytocin for induction of labor at term with intact membranes and an unripe cervix to two simultaneous regimens. Our aim was to confirm findings from smaller trials and add to data on fetal safety.
What is the current status of trial NCT00504465?
This trial is currently completed. It is a NA study. The enrollment target is 210 participants. The study started on 2002-05. Estimated completion is 2007-04.
What interventions are being tested in trial NCT00504465?
The interventions under investigation include: dinoprostone (DRUG).
Who is sponsoring clinical trial NCT00504465?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00504465's enrollment target sits among peer trials
210 490th of 2000 higher than 1,505 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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