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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 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.
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 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06702670
The ClinicalTrials.gov registry entry for NCT06702670 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Treatment with Diphenhydramine is the first listed.
NCT06702670 reports 0 study locations.
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.
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