drugset / Trial / NCT02726971

Comparison of Different Doses of Oestrogen Therapy for Preventing Intrauterine Adhesion

NCT02726971

Phase 1/2 Completed 141 enrolled Fu Xing Hospital, Capital Medical University
RandomizedParallel-groupSingle-blindPrevention

Summary

This single-center,prospective,randomized,controlled trial is conducted to evaluate the efficacy of different doses of estrogen artificial periodic therapy after hysteroscopic adhesiolysis in patients with moderate-severe adhesion.

Timeline

Start
2016-04
Primary completion
2016-08
Completion
2016-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Dydrogesterone Other / unclassified 10 mg Oral
Subject Dydrogesterone Other / unclassified 20 mg Oral
Subject Estradiol Other / unclassified 2 mg Oral
Subject Estradiol Other / unclassified 4 mg Oral
Subject Estradiol Other / unclassified 6 mg Oral

Indications