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

Study:

n/a

Rationale:

n/a

Purpose:

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

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
ClinicalTrials.gov 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

This information is abridged to display results relevant only to Cleveland Clinic. To see complete record visit ClinicalTrials.gov
  Information obtained from ClinicalTrials.gov on
Link to the current ClinicalTrials.gov record.

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