drugset / Trial / NCT02901561

Comparison Between 2 Doses of Misoprostol Before Intrauterine Device

NCT02901561

Phase 2/3 Completed 212 enrolled Assiut University
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of the investigators' study was to evaluate whether misoprostol will improve pain scores .

Timeline

Start
2016-09
Primary completion
2016-12
Completion
2017-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Misoprostol Other / unclassified 200 ug Intravenous
Subject Misoprostol Other / unclassified 400 ug Intravenous

Indications

No indication recorded.