drugset / Trial / NCT00363389

Hysteroscopy and Misoprostol Project

NCT00363389

Phase 3 Completed 86 enrolled Ullevaal University Hospital
RandomizedParallel-groupDouble-blindTreatment

Summary

To investigate if self-inserted vaginal misoprostol prior to outpatient hysteroscopy will lead to satisfactory cervical ripening, compared to placebo.

Timeline

Start
2006-09
Primary completion
Completion
2007-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Misoprostol Other / unclassified 1000 ug Intrathecal

Indications