drugset / Trial / NCT05262738

Misoprostol Dosing in BMI Greater Than 30

NCT05262738 ↗

Phase 4 Completed 180 enrolled University of Texas at Austin
RandomizedParallel-groupDouble-blindTreatment

Summary

The investigators are performing a randomized controlled-trial investigating if 50mcg (compared to 25 mcg) of vaginal misoprostol reduces the time from induction start to delivery in obese women.

Timeline

Start
2022-06-01
Primary completion
2023-07-14
Completion
2023-07-17

Outcome

Missed primary endpoint

paper No difference was found in the primary outcome of time to delivery (21.6 hours vs 18.6 hours; PMID 38367750 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Misoprostol Other / unclassified 25 ug Intravitreal
Subject Misoprostol Other / unclassified 50 ug Intravitreal