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NCT06702670: ACCEL

Anticholinergics for Cervical Edema in Labor

Not yet recruiting Phase 2, PHASE3 Last updated 25 November 2024
What this trial tests

Phase 2, PHASE3 trial testing Treatment with Diphenhydramine in Labor Dystocia in 200 participants. Not yet recruiting.

Timeline
1 December 2024
Primary endpoint
1 December 2025
14 December 2025

Quick facts

Lead sponsorThe University of Texas Health Science Center, Houston
PhasePhase 2, PHASE3
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment200
Start date1 December 2024
Primary completion1 December 2025
Estimated completion14 December 2025
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

The University of Texas Health Science Center, Houston

Who can join

18 and older, female only, with Labor Dystocia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Labor Dystocia

Currently open trials in the same condition.

Other The University of Texas Health Science Center, Houston trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06702670.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing