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RECRUITING
NCT07517796
PHASE4

I.V Papavrine for Labor Induction in Term PROM

Sponsor: Western Galilee Hospital-Nahariya

View on ClinicalTrials.gov

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

Official title: I.V Papavrine for Labor Induction in Term PROM: A Prospective Randomized Controlled Trial

Key Details

Gender

FEMALE

Age Range

18 Years - 45 Years

Study Type

INTERVENTIONAL

Enrollment

110

Start Date

2025-10-22

Completion Date

2027-10-22

Last Updated

2026-04-08

Healthy Volunteers

Yes

Interventions

DRUG

Papaverine arm

given 12 houres after rupture of membranes

OTHER

Placebo

I.V seline

Locations (1)

Galilee Medical Center

Nahariya, Israel, Israel