drugset / Trial / NCT01754649

Use of Misoprostol in Case of Insertion Failure of Intrauterine Contraceptives

NCT01754649

Phase 4 Completed 102 enrolled Luis Bahamondes
RandomizedParallel-groupDouble-blindTreatment

Summary

To assess the usefulnes sof misoprostol versus placebo (in a double-blind placebo controlled randomized clinical trial)to facilitate the insertion of copper-IUD and the levonorgestrel-releasing intrauterine system (LNG-IUS) in cases of failure due to cervical stenosis in either nulligravidas and parous women. Additionally to evaluate the side-effects of the misoprostol. The hypothesis is that misoprostol may be better than placebo.

Timeline

Start
2013-01
Primary completion
2014-12
Completion
2014-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Misoprostol Other / unclassified 200 ug Other

Indications

No indication recorded.