drugset / Trial / NCT02824224

Tamoxifen to Reduce Unscheduled Bleeding in New Users of the Levonorgestrel-releasing Intrauterine System (LNG-IUS)

NCT02824224

Phase 4 Completed 42 enrolled Oregon Health and Science University
RandomizedParallel-groupDouble-blindPrevention

Summary

This study evaluates the ability of tamoxifen to improve frequent or prolonged bleeding in new users of the 52mg levonorgestrel-releasing intrauterine device (IUD). Half of participants will receive a course of tamoxifen three weeks after insertion of the IUD, while the other half of participants will receive a course of placebo.

Timeline

Start
2016-09-06
Primary completion
2018-01-08
Completion
2018-01-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Tamoxifen Small molecule 10 mg Oral