Ignite Creation Date:
2025-12-25 @ 3:07 AM
Ignite Modification Date:
2025-12-26 @ 1:46 AM
Study NCT ID:
NCT05981833
Status:
RECRUITING
Last Update Posted:
2025-02-24
First Post:
2023-08-01
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Dermal Allograft Augmentation of Large and Massive Rotator Cuff Tears
Sponsor:
Arthrex, Inc.
Organization:
Study Overview
Official Title:
A Randomized, Post-market Study Evaluating Dermal Allograft Augmentation of Large and Massive Rotator Cuff Tears
Status:
RECRUITING
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to compare postoperative healing of large and massive rotator cuff tears with preoperative MRI confirmed fatty infiltration stage II and higher repaired with or without dermal allograft augmentation (DAA).
Detailed Description:
The primary objective is to evaluate postoperative healing of rotator cuff repair with and without DAA.
Primary: The primary outcome measure is healing evaluation in MRI . MRI Post-Operative Assessment (Goutallier Stage and Sugaya Classification)
Secondary: The secondary outcome measures are patient-reported outcome measures from validated outcome scoring systems, including:
American Shoulder and Elbow Surgeons Score (ASES)
Single Assessment Numeric Evaluation score (SANE)
Visual Analog Scale (VAS) for pain
Veterans RAND Health Survey (VR-12)
Population: Males and females between the ages of 30 and 75 years that require surgery for large and massive rotator cuff tears
Description of Treatment: Rotator cuff repair with or without augmentation using decellularized human dermal allograft.
Primary: The primary outcome measure is healing evaluation in MRI . MRI Post-Operative Assessment (Goutallier Stage and Sugaya Classification)
Secondary: The secondary outcome measures are patient-reported outcome measures from validated outcome scoring systems, including:
American Shoulder and Elbow Surgeons Score (ASES)
Single Assessment Numeric Evaluation score (SANE)
Visual Analog Scale (VAS) for pain
Veterans RAND Health Survey (VR-12)
Population: Males and females between the ages of 30 and 75 years that require surgery for large and massive rotator cuff tears
Description of Treatment: Rotator cuff repair with or without augmentation using decellularized human dermal allograft.
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?: