drugset / Trial / NCT04132349

Ulipristal Acetate in Symptomatic Uterine Fibroid

NCT04132349

Phase 4 Terminated 25 enrolled My Duc Hospital
NaSingle-groupOpen-labelTreatment

Summary

This study evaluates the effectiveness and safety of ulipristal acetae (UPA) in women with symptomatic uterine fibroids. Those who fulfilled inclusion/exclusion criteria will be treated UPA at daily dose of 5mg.

Timeline

Start
2019-10-23
Primary completion
2020-04-01
Completion
2020-04-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Ulipristal Acetate Unknown 5 mg Oral

Indications