Expired Study
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New York, New York 10021


Purpose:

The purpose of this study is to allow patients to undergo surgery with the SR™ PIP (Proximal Interphalangeal) Implants for finger arthritis. This is NOT a research study, but rather, a requirement by the FDA for humanitarian use of device


Study summary:

The purpose of this IRB approved study is to allow patients to undergo surgery with the SR™ PIP (Proximal Interphalangeal) Implants. This is NOT a research study, but rather, a requirement by the FDA for humanitarian use of device. Use of the SR™ PIP is approved for humanitarian use by the FDA when either the patient is in need of a revision of failed PIP prothesis(es) or the patient expects to place his/her hand under loading situation which preclude the use of an alternative implant in the painful osteo-arthritic and post traumatic arthritic PIP joint.


Criteria:

Inclusion Criteria: - patient is in need of a revision of failed PIP prosthesis(es) - patient expects to place his/her hands under loading situations which preclude the use of an alternative implant in the painful osteo-arthritic and post traumatic arthritic PIP joint Exclusion Criteria: - patient is not in need of a revision of a failed PIP prothesis(es) - patient is eligible to use an alternative implant


NCT ID:

NCT02244788


Primary Contact:

Sophia Paul, BA
Phone: 212-774-2440
Email: pauls@hss.edu


Backup Contact:

N/A


Location Contact:

New York, New York 10021
United States

Sophia Paul, BA
Phone: 212-774-2440
Email: pauls@hss.edu

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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