Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Birth Control
  • Breakthrough Bleeding
  • Contraception
  • Implant
  • Uterine Bleeding
Type
Interventional
Phase
Phase 4
Design
Allocation: RandomizedIntervention Model: Crossover AssignmentMasking: Triple (Participant, Care Provider, Investigator)Primary Purpose: Treatment

Participation Requirements

Age
Between 14 years and 48 years
Gender
Only males

Description

The purpose of this study is to find out what effects norethindrone acetate (NTA) has on the duration and recurrence of frequent and/or prolonged bleeding associated with Nexplanon™.

The purpose of this study is to find out what effects norethindrone acetate (NTA) has on the duration and recurrence of frequent and/or prolonged bleeding associated with Nexplanon™.

Tracking Information

NCT #
NCT04676061
Collaborators
Merck Sharp & Dohme Corp.
Investigators
Principal Investigator: Joanna Stacey, MD Baylor Reserach Institute