Registry of Amniotic Membrane: Evaluating Utilization and Outcomes in Various Applications

Completed

Conditions studied: Orthopedic Disorder, Wound

In brief

This registry will assess clinical outcomes following the use of Cryopreserved Amniotic Membrane (CAM) for the treatment of orthopedic and various other conditions. This registry will collect outcomes data via a registry of up to 100 patients who have received treatment with CAM in the post-market setting. Patients will be enrolled from up to five healthcare centers.

Key facts

Study ID

NCT04222166

Run by

MED Institute Inc.

People needed

100

Starts

2019-12-16

Expected to finish

2021-08-06

Last updated by the study team

2021-08-27

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• A patient is suitable for inclusion in this registry if the patient has been treated with CAM for any indication as per the standard of care practice.

You may not qualify if…

• Patients are excluded from registry enrollment if they are under the age of 22 years.

Where it is running

• Regenerative Medicine and Pain Management Physicians — Gulf Breeze, Florida, United States
• Foot and Ankle Specialists of South Jersey — Voorhees Township, New Jersey, United States

Full record on ClinicalTrials.gov

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