Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT06702670 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Anticholinergics for Cervical Edema in Labor

Study acronym: ACCEL
StatusRecruiting
PhasePhase 2/3
Started2025-03-25
View on ClinicalTrials.gov ↗

Amendment history

2026-05-04
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Primary completion date2025-12-01→2027-03-25
Completion date2025-12-14→2027-04-09
Start dateestimated 2024-12-01→confirmed 2025-03-25
Study sitesdetails revised at 1 of 1 site
2024-11-20
minor
Original filing
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.
Trial Details
NCT Number NCT06702670
Lead Sponsor The University of Texas Health Science Center, Houston
Conditions Labor Dystocia
Enrollment 200 participants
Start Date 2025-03-25
Primary Completion 2027-03-25 (estimated)
Study Completion 2027-04-09 (estimated)
Updated on ClinicalTrials.gov 2026-05-06