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A Pilot Study to Evaluate the Safety and Efficacy of Amniotic Membrane Transplantation in Patients with Arthrofibrosis following Total Knee Arthroplasty

IRB Number: 2015-069
not enrolling new patients

August 18, 2014

Institutional Review Board, Hospital for Special Surgery

The safety of our participants is our top priority. The trial/study is approved and periodically reviewed by the Institutional Review Board (IRB), which includes doctors, administrators, ethicists, and members of the general public. The safety of clinical trials is reviewed by the U.S. Food and Drug Administration.

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Principal Investigator

David J. Mayman, MD

Co-Investigators

Seth A. Jerabek, MD
Kaitlin M. Carroll

Summary

5 patients, and 6 month’s post operatively for follow-up.

Inclusion/Exclusion Criteria

  • Inclusion Criteria: (1) Patients with mature arthrofibrosis who are a minimum of 1 year post TKA and (2) Documented flexion less than 90 degrees.
  • Exclusion Criteria: Patients that are wheelchair bound.

Contact Information

David J. Mayman, MD
maymand@hss.edu
212.774.2024