drugset / Trial / NCT06726278

Significance of Misoprostol-induced Cervical Ripening Prior to Hysteroscopy

NCT06726278

RandomizedParallel-groupQuadruple-blindHealth-services research

Summary

The goal of this prospective study is to evaluate the efficacy and safety of misoprostol for cervical ripening prior to hysteroscopy

Timeline

Start
2022-08-01
Primary completion
2024-07-30
Completion
2024-07-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Misoprostol Other / unclassified 400 ug Intrathecal

Indications