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Use Misoprostol to Optimize Prevention of Cervical Cancer

Study acronym: MISOPCx
StatusRecruiting
PhaseNot applicable
Started2025-02-25
View on ClinicalTrials.gov ↗
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.

Amendment history 2 changes detected by DataLookout

2026-09-01
critical
Primary completion pushed: 2026-11-04 → 2027-11-04
2026-09-01
minor
Completion pushed: 2027-11-04 → 2028-11-11
Trial Details
NCT Number NCT06669533
Lead Sponsor University of Alabama at Birmingham
Collaborators: Cameroon Baptist Convention Health, National Cancer Institute (NCI)
Conditions Cervical Cancers
Enrollment 420 participants
Start Date 2025-02-25
Primary Completion 2027-11-04 (estimated)
Study Completion 2028-11-11 (estimated)
Updated on ClinicalTrials.gov 2026-08-31