drugset / Trial / NCT00725413

A Study to Investigate the Contraceptive Efficacy and Safety of a Subdermal Etonogestrel Implant (Implanon®)(P06473)(COMPLETED)

NCT00725413

Phase 4 Completed 210 enrolled Organon and Co
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to investigate the contraceptive efficacy, safety and acceptability of Organon's subdermal etonogestrel implant in healthy female volunteers in various countries in order to obtain country-specific data.

Timeline

Start
2001-11
Primary completion
2005-11
Completion
2005-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Etonogestrel Unknown Other

Indications

No indication recorded.