drugset / Trial / NCT03642210

Study of a Levonorgestrel 52 mg Intrauterine System for the Treatment of Heavy Menstrual Bleeding

NCT03642210

Phase 3 Completed 105 enrolled Medicines360
NaSingle-groupOpen-labelTreatment

Summary

To assess the efficacy of a levonorgestrel 52 mg intrauterine system as a treatment for heavy menstrual bleeding.

Timeline

Start
2019-01-17
Primary completion
2021-10-12
Completion
2021-10-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Levonorgestrel Small molecule 52 mg Other

Indications