drugset / Trial / NCT03683914

Vaginal Dinoprostone Prior to Diagnostic Office Hysteroscopy in Postmenopausal Patients

NCT03683914

Phase 4 Completed 102 enrolled Cairo University
RandomizedParallel-groupDouble-blindTreatment

Summary

To compare the effectiveness of vaginal dinoprostone with placebo in minimising the pain experienced by postmenopausal patients during diagnostic office hysteroscopy and to assess the ease of insertion of hysteroscope as reported by the hysteroscopist.

Timeline

Start
2018-09-30
Primary completion
2019-01-30
Completion
2019-02-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Dinoprostone Other / unclassified 3 mg Intravenous

Indications

No indication recorded.