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Axis™ Allograft Dermis for Female Pelvic Floor Repair: a Prospective Post Market Study






This study is a prospective, single arm, multi-center, post-market study to evaluate the efficacy of Axis™ Allograft Dermis used for anterior, posterior or combined (anterior and posterior) pelvic organ prolapse repair.

Study Status: Recruiting

Calvin Killingbeck 954-659-6247

Condition Intervention Phase
Pelvic Organ Prolapse Other: Axis N/A

Verified by Coloplast A/S July, 2013

Sponsored by: Coloplast A/S
Information provided by: Coloplast A/S identifier: NCT01541748

Study Type: Interventional

Study Design: Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Cleveland Clinic Florida
Weston, Florida 33331
United States

Kristine Whitmore, MD., Principal Investigator

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