Zimmer Knee Creations SCP® Observational Cohort Follow-Up Study
Status: Completed
Location: See all (14) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
Post Market clinical outcomes study to collect data on the short - and long-term outcomes for subjects who are undergoing or who have undergone the Subchondroplasty (SCP) Procedure in the knee in a standard clinical setting. Outcomes to be assessed include pain medication usage, pain, function, activity levels and patient satisfaction.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Surgeon considers patient appropriate for SCP procedure.
• Patient has agreed to undergo the SCP procedure or has already undergone the procedure.
• Subject is willing and able to sign a written consent form.
• The subject has the mental capacity and the willingness to contribute follow-up outcome data.
• Patient is willing and able to complete outcome forms in person or by phone, email or regular mail.
Locations
United States
Colorado
Denver-Vail Orthopedics
Parker
Florida
Atlantis Orthopaedics
Palm Beach Gardens
Foundation for Orthopaedic Research and Education (FORE)
Tampa
Georgia
Southern Ortho
Johns Creek
Indiana
OrthoIndy
Indianapolis
Louisiana
Cascio Sports Medicine
Lake Charles
Massachusetts
Brigham and Women's Hospital
Boston
Orthopaedic Surgical Associates
North Chelmsford
Michigan
Beaumont Health System
Royal Oak
Associated Orthopedists
Saint Clair Shores
New York
New York University School of Medicine
Huntington Station
Ohio
Ohio State University
Columbus
Pennsylvania
Allegheny Singer Research Institute
Pittsburgh
Virginia
Jordan-Young Institute
Virginia Beach
Time Frame
Start Date: 2012-09-18
Completion Date: 2023-05-31
Participants
Target number of participants: 516
Authors
Sponsors
Leads: Zimmer Biomet