Last updated on November 2018

A Study to Evaluate the Effectiveness of Essure Post-NovaSure Radiofrequency Endometrial Ablation Procedure Following a Successful Essure Confirmation Test


Brief description of study

The purpose of the post approval study is to evaluate the effectiveness and safety of the Essure System when a NovaSure Endometrial Ablation procedure is performed following a successful Essure Confirmation Test.

Detailed Study Description

This study has previously been posted by Conceptus, Inc. After acquiring Conceptus, Inc., Bayer is now the sponsor of the trial.

Clinical Study Identifier: NCT01740687

Contact Investigators or Research Sites near you

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Bayer Clinical Trials Contact

Englewood, OH United States

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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