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NCT06702670 · ClinicalTrials.gov registry record · Phase 2
Anticholinergics for Cervical Edema in Labor
A Phase 2 study, sponsored by The University of Texas Health Science Center, Houston.
- Recruiting
- Registry status
- Phase 2
- Development phase
- 200
- Enrollment target
NCT06702670: Recruiting Phase 2 study, sponsored by The University of Texas Health Science Center, Houston.
NCT06702670 is a Phase 2 study that is actively recruiting participants, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 200 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06702670, a Phase 2 study, is actively recruiting participants, sponsored by The University of Texas Health Science Center, Houston.
- RECRUITING
- Registry status
- Phase 2
- Development phase
- 200 participants
- Enrollment target
Study Summary
The purpose of this study is to is to determine the clinical effectiveness of a single dose of intravenous (IV) medication for the prevention of labor arrest and cesarean delivery in primiparous women undergoing trial of labor.
Interventions
- DRUG Treatment with Diphenhydramine
- COMBINATION_PRODUCT Usual Care
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2025-03-25 |
| Est. Completion | 2027-04-09 |
| Phase | Phase 2 |
What NCT06702670 shows while recruiting
NCT06702670 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% higher).
The record links to 0 conditions, and to 2 interventions - of which Treatment with Diphenhydramine is the first listed.
NCT06702670 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06702670 about?
NCT06702670 is a clinical study titled "Anticholinergics for Cervical Edema in Labor". The purpose of this study is to is to determine the clinical effectiveness of a single dose of intravenous (IV) medication for the prevention of labor arrest and cesarean delivery in primiparous women undergoing trial of labor.
What is the current status of trial NCT06702670?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 200 participants. The study started on 2025-03-25. Estimated completion is 2027-04-09.
What interventions are being tested in trial NCT06702670?
The interventions under investigation include: Treatment with Diphenhydramine (DRUG), Usual Care (COMBINATION_PRODUCT).
Who is sponsoring clinical trial NCT06702670?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06702670's enrollment target sits among peer trials
200 304th of 2000 higher than 1,652 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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