drugset / Trial / NCT03790371

Vaginal Misoprostol Before Intrauterine Contraceptive Device Insertion

NCT03790371

Phase 3 Completed 90 enrolled Ain Shams University
RandomizedParallel-groupTriple-blindTreatment

Summary

the current study was conducted to assess efficacy of vaginal misoprostol before IUD insertion following previous insertion failure

Timeline

Start
2015-10-01
Primary completion
2016-08-01
Completion
2016-08-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Misoprostol Other / unclassified 200 ug Other

Indications

No indication recorded.