A Surgical Simulation Study to Evaluate the Safety of a Device Mechanism as Treatment for Vaginal Apical Prolapse
NCT00965952 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 49
Last updated 2010-02-10
Summary
The purpose of this pilot study is to perform a procedure to evaluate the safety of the placement of a new device (known as the VFIX device).
Conditions
- Pelvic Organ Prolapse
Sponsors & Collaborators
-
Ethicon, Inc.
lead INDUSTRY
Principal Investigators
-
David Robinson, MD · Ethicon, Inc.
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-07-31
- Primary Completion
- 2009-12-31
- Completion
- 2009-12-31
Countries
- Australia
Study Locations
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