InSpace Accelerated Rehabilitation Study
NCT05329584
This study is recruiting at 11 US sites in 10 states, according to its ClinicalTrials.gov record last updated .
Summary
This is a prospective, parallel group, open-label, multi- center, randomized study to assess two accelerated rehabilitation programs for use with the InSpace device in the treatment of full thickness Massive, Irreparable Rotator Cuff Tears (MIRCTs) performed during an arthroscopic procedure.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Rotator Cuff Tears
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 65 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Sponsor
- Stryker Endoscopy
- Last updated on ClinicalTrials.gov
- May 29, 2025
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Arizona · 1
- Musculoskeletal-Orthopedic Research and Education Foundation · Phoenix, AZ
Arkansas · 1
- University of Arkansas for Medical Sciences · Little Rock, AR
Colorado · 1
- Steadman Hawkins Clinic Denver · Englewood, CO
Florida · 2
- Holy Cross Hospital · Fort Lauderdale, FL
- Paley Orthopaedics & Spine · West Palm Beach, FL
Georgia · 1
- Emory University · Atlanta, GA
Illinois · 1
- Rush University Medical Center · Chicago, IL
Minnesota · 1
- Mayo Clinic · Rochester, MN
New York · 1
- Hospital for Special Surgery · New York, NY
Pennsylvania · 1
- The Rothman Institute · Philadelphia, PA
Texas · 1
- TSAOG Orthopaedics & Spine · San Antonio, TX
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.