drugset / Trial / NCT06669533

Use Misoprostol to Optimize Prevention of Cervical Cancer

NCT06669533

RandomizedSingle-groupOpen-labelScreening

Summary

This is a double-blind randomized controlled trial of 420 non-pregnant women undergoing cancer screening by visual inspection with acetic acid (VIA) who have Type 3 transformation zone (TZ) and randomized to receive either Misoprostol or placebo.

Timeline

Start
2025-02-25
Primary completion
2026-11-04
Completion
2027-11-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Misoprostol Other / unclassified 600 ug Other

Indications