Allograft Reconstruction of Massive Rotator Cuff Tears vs Partial Repair Alone
Primary Purpose
Rotator Cuff Syndrome, Rotator Cuff Injury, Disorder of Rotator Cuff
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Partial Rotator Cuff Repair
Partial Rotator Cuff Repair with Allograft Augmentation
Sponsored by
About this trial
This is an interventional treatment trial for Rotator Cuff Syndrome
Eligibility Criteria
Inclusion Criteria:
- Large/Massive rotator cuff tear >3cm proven on MRI
Exclusion Criteria:
- Non surgical candidate, unable to consent
Sites / Locations
- Nova Scotia Health Authority
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Partial Repair / Debridement
Allograft Reconstruction
Arm Description
Subjects in this arm of the study will receive the intervention "Partial Rotator Cuff Repair". This is the control group.
Subjects in this arm of the study will receive the intervention "Partial Rotator Cuff Repair with Allograft Augmentation"
Outcomes
Primary Outcome Measures
Western Ontario Rotator Cuff (WORC) Index
A patient questionnaire evaluating shoulder pain, function.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01987973
Brief Title
Allograft Reconstruction of Massive Rotator Cuff Tears vs Partial Repair Alone
Official Title
Arthroscopic Repair of Chronic Two-tendon Rotator Cuff Tears by Human Dermal Allograft
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
February 2015 (undefined)
Primary Completion Date
December 2019 (Actual)
Study Completion Date
March 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Ivan Wong
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The investigators hypothesize that the use of an allograft adjuvant to partial repair will lead to improved shoulder outcome measure scores compared to partial repair alone in massive rotator cuff tears.
Detailed Description
A total of 30 patients will be enrolled in the study. Subjects will be randomized into two arms, either (1) Partial Repair/Debridement or (2) Allograft Reconstruction.
The patients will complete a structured clinical examination conducted by a sports medicine fellowship trained orthopaedic consultant, Pre-operatively and Post-operatively at 6 weeks, 3, 6, 12, 24 months. The examination will consist of range of motion testing by goniometer as well as strength testing by hand dynamometer. The patient will also complete the Western Ontario Rotator Cuff Index (WORC) questionnaire.
The main benefit of this procedure is that patients who have currently irreparable massive, chronic rotator cuff tears may acquire a means for their cuff to be repaired. This may aid in improving function of the shoulder, restoring ability to complete activities of daily living, while decreasing pain and sleep disturbances. This would allow the participant to become more functional after rehabilitation. It is our belief that this study could provide new information in helping to understand this relationship, which would in turn lead to future study in this area of orthopaedic surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotator Cuff Syndrome, Rotator Cuff Injury, Disorder of Rotator Cuff, Full Thickness Rotator Cuff Tear, Skin Graft (Allograft) (Autograft) Failure
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
29 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Partial Repair / Debridement
Arm Type
Active Comparator
Arm Description
Subjects in this arm of the study will receive the intervention "Partial Rotator Cuff Repair". This is the control group.
Arm Title
Allograft Reconstruction
Arm Type
Experimental
Arm Description
Subjects in this arm of the study will receive the intervention "Partial Rotator Cuff Repair with Allograft Augmentation"
Intervention Type
Procedure
Intervention Name(s)
Partial Rotator Cuff Repair
Other Intervention Name(s)
Debridement
Intervention Description
This is the control group. The bursa will be debrided thoroughly and rotator cuff edges will be shaved down to stable tissue. If possible, rip-stop sutures will be employed to stabilize the tear. The subacromial space will then be thoroughly irrigated.
Intervention Type
Procedure
Intervention Name(s)
Partial Rotator Cuff Repair with Allograft Augmentation
Other Intervention Name(s)
Human dermal allograft, Allograft Reconstruction
Intervention Description
Patients in this arm will undergo a partial rotator cuff repair (debridement), followed by an allograft augmentation. An Allopatch HD patch will be rehydrated in saline solution for 15 minutes. The patch is then sewn in place with braided polyester suture material. Multiple sutures, approximately 5 to 10 mm apart from one another will be used. The medial sutures are placed at least 3 cm medial to the tendon-bone attachment site. The patch is stretched to remove the manufacturing surface irregularities. The patch is then attached to the greater tuberosity at the tendon-bone attachment site with arthroscopic bone anchors. The subacromial space will then be thoroughly irrigated.
Primary Outcome Measure Information:
Title
Western Ontario Rotator Cuff (WORC) Index
Description
A patient questionnaire evaluating shoulder pain, function.
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Large/Massive rotator cuff tear >3cm proven on MRI
Exclusion Criteria:
Non surgical candidate, unable to consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ivan H Wong, MD FRCS(C)
Organizational Affiliation
Nova Scotia Health Authority
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nova Scotia Health Authority
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3H2E1
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34494901
Citation
Wong I, Sparavalo S, King JP, Coady CM. Bridging Allograft Reconstruction Is Superior to Maximal Repair for the Treatment of Chronic, Massive Rotator Cuff Tears: Results of a Prospective, Randomized Controlled Trial. Am J Sports Med. 2021 Oct;49(12):3173-3183. doi: 10.1177/03635465211039846. Epub 2021 Sep 8.
Results Reference
derived
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Allograft Reconstruction of Massive Rotator Cuff Tears vs Partial Repair Alone
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