drugset / Trial / NCT07517796

I.V Papavrine for Labor Induction in Term PROM

NCT07517796

Phase 4 Recruiting 110 enrolled Western Galilee Hospital-Nahariya
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This prospective randomized controlled trial aims to evaluate whether intravenous administration of papaverine 12 hours after term PROM reduces the interval from membrane rupture to delivery and improves maternal and neonatal outcomes. Researchers will compare drug papaverine to a placebo

Timeline

Start
2025-10-22
Primary completion
2027-10-22
Completion
2027-10-22

Drugs

EvaluationDrugModalityDoseRoute
Comparator Papaverine Small molecule 80 mg Intravenous