ESS505 Pre-hysterectomy Protocol

Status Completed

Clinical Trial Summary

This study has been designed to evaluate an investigational model of the Essure System for Permanent Birth Control. The investigational device is designed to offer all the advantages of the currently approved device. In addition, the investigational device offers immediate, permanent contraception without a three-month waiting period or 90-day confirmation test. This study has been designed to evaluate the effectiveness of the investigational device in causing tubal occlusion from insert placement through three months of wearing.

Clinical Trial Description

This study has previously been posted by Conceptus, Inc. (US).

After acquiring Conceptus, Inc., Bayer HealthCare AG (Germany) is the sponsor of the trial. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label

Related Conditions & MeSH terms

Contraception

Clinical Trial Details

NCT number	NCT01664052
Study type	Interventional
Source	Bayer
Contact
Status	Completed
Phase	N/A
Start date	July 2012
Completion date	March 2013

View Details

See also
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