Evaluating Post-Operative Outcomes in Patients with Charcot Foot with Ankle/Hindfoot Reconstruction

Full Title of Study

Evaluating Post-Operative Outcomes in Patients with Charcot Foot with Ankle/Hindfoot Reconstruction (R# 11-01382)

Purpose of Study

To compare foot function, motion and pressure in individuals who have had surgical reconstruction of the foot and control subjects.

Basic Inclusion Criteria (requirements for being included in study)

  • Age 18 years or older
  • Had surgery for a diabetic Charcot foot 
  • OR is a control subject, matched in age and gender to a patient

Basic Exclusion Criteria (reasons for being excluded from study)

  • Inability to walk independently
  • Uncontrolled cardiovascular or neuromusculoskeletal disease

Study Visit Requirements

One visit lasting 60-75 minutes

Principal Investigators

Kenneth Mroczek, MD

Smita Rao, PT, PhD

Answers to frequently asked questions (FAQs) about clinical trials

For more information about enrolling in this study, please contact Smita Rao, smita.rao@nyumc.org