drugset / Trial / NCT07641543

Papaverine for Prevention of Perineal Trauma

NCT07641543

Not yet recruiting 412 enrolled Dr Raneen Abu Shqara
RandomizedParallel-groupQuadruple-blindPrevention

Summary

Perineal trauma is a common complication of vaginal delivery, particularly among primiparous patients, and may result in short- and long-term maternal morbidity, including pain, dyspareunia, and pelvic floor dysfunction. Papaverine hydrochloride, a smooth muscle relaxant with vasodilatory properties, has been shown to improve tissue relaxation and has been used safely in obstetric settings. This prospective randomized double-blind placebo-controlled study aims to evaluate whether intrapartum intravenous papaverine hydrochloride (80 mg), administered at full cervical dilatation, reduces the rate of perineal trauma among primiparous patients undergoing vaginal delivery. Eligible participants will be randomized in a 1:1 ratio to receive either intravenous papaverine hydrochloride or placebo (normal saline). Maternal, obstetric, and neonatal outcomes, including the rate and severity of perineal trauma, obstetric anal sphincter injuries (OASIS), postpartum hemorrhage, and neonatal outcomes, will be assessed.

Timeline

Start
2026-06-03
Primary completion
2027-06-03
Completion
2027-06-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Papaverine Small molecule 80 mg Intravenous