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A Randomized Clinical Trial Comparing Open to Mini-Open Rotator Cuff Repair for Full-Thickness Rotator Cuff Tears.

Primary Purpose

Rotator Cuff Tear

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Open acromioplasty with rotator cuff repair
Arthroscopic acromioplasty with mini-open repair
Sponsored by
University of Calgary
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rotator Cuff Tear focused on measuring rotator cuff, open, arthroscopic, mini-open, acromioplasty, quality of life, shoulder

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients with unremitting pain in the affected shoulder who have failed conservative treatment for at least 3 months Weakness of rotator cuff (MRC grades 4-, 4 or 4+) Positive diagnostic imaging on the affected shoulder indicating a full-thickness rotator cuff tear which may include arthrogram, ultrasound or MRI Age > 18 years English speaking Exclusion Criteria: A massive rotator cuff tear as demonstrated by Grade 3 or less muscle strength on testing internal and external rotation of the affected shoulder Previous surgery to the affected shoulder

Sites / Locations

  • University of Calgary Sport Medicine Centre
  • Royal Columbian Hospital
  • Fowler Kennedy Sport Medicine Centre
  • Sunnybrook and Women's College Health Sciences Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Open Repair

Mini-open Repair

Arm Description

Outcomes

Primary Outcome Measures

Rotator Cuff Quality of Life Questionnaire (RC-QOL)

Secondary Outcome Measures

American Shoulder and Elbow Surgeons Score
Shoulder Rating Questionnaire
Functional Shoulder Elevation Test
Range of motion
Strength

Full Information

First Posted
November 7, 2005
Last Updated
January 14, 2008
Sponsor
University of Calgary
Collaborators
Workers' Compensation Board, Alberta, Canadian Orthopaedic Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00251147
Brief Title
A Randomized Clinical Trial Comparing Open to Mini-Open Rotator Cuff Repair for Full-Thickness Rotator Cuff Tears.
Official Title
Prospective Randomized Study Comparing Open Acromioplasty and Rotator Cuff Repair Versus Arthroscopic Acromioplasty and Mini-Open Rotator Cuff Repair.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2008
Overall Recruitment Status
Completed
Study Start Date
March 1999 (undefined)
Primary Completion Date
October 2005 (Actual)
Study Completion Date
October 2005 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Calgary
Collaborators
Workers' Compensation Board, Alberta, Canadian Orthopaedic Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study compares standard open rotator cuff repair versus arthroscopic mini-open rotator cuff repair by measuring the disease-specific quality of life at 2 years in patients with full thickness rotator cuff tears. Hypothesis: There is no difference in disease-specific quality of life outcome at two years between open versus arthroscopic mini-open repair for patients with full-thickness rotator cuff tears.
Detailed Description
Rotator cuff injury affects a diverse group of patients and leads to significant disability with respect to lost time from work and the inability to play sports, thereby affecting the individual's quality of life. The standard treatment for full-thickness rotator cuff repair is with an open acromioplasty procedure. An alternative procedure for a full-thickness rotator cuff tear is with a combined procedure of arthroscopic acromioplasty and mini-open repair, which has the potential advantages of a preserved deltoid origin, lower perioperative morbidity, shorter hospital stays and less soft tissue dissection. The progression towards arthroscopic repair requires a comparison to the standard, open procedure for full-thickness rotator cuff tears, using validated outcomes in a randomized fashion. This study is designed as a multi-centre randomized controlled trial with a priori sample size calculation of 28 patients per group. Patients presenting with unremitting pain, failed conservative treatment of at least 3 months, weakness of the rotator cuff and positive imaging indicating a full-thickness rotator cuff tear are eligible for the study. Previous surgery on the affected shoulder and massive rotator cuff tears are excluded. Patients are randomized using computer-generated block randomization, stratified by surgeon, to either open or mini-open rotator cuff repair. Disease-specific quality of life is assessed using the validated Rotator Cuff Quality of Life Questionnaire, a self-administered, 34-item questionnaire designed specifically to assess patients before and after surgery. It utilizes a visual analog scale scored out of 100, with a higher score reflecting a better quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotator Cuff Tear
Keywords
rotator cuff, open, arthroscopic, mini-open, acromioplasty, quality of life, shoulder

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
73 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Open Repair
Arm Type
Active Comparator
Arm Title
Mini-open Repair
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Open acromioplasty with rotator cuff repair
Other Intervention Name(s)
Open repair
Intervention Description
A standard vertical incision was made over the anterolateral aspect of the acromion. The deltoid muscle was split and stripped off the anterior aspect of the acromion. The anterior and inferior aspect of the acromion was removed. The coracoacromial ligament was excised. Repair of the tear in the cuff tendon(s) was accomplished by suturing leading edge of the tear into the greater tuberosity of the humerus at or near the original site of insertion of the cuff to bone. Trans-osseous sutures, suture anchors and tendon to tendon suture repair techniques were employed for a secure repair with the arm at the side. The surgeon was allowed to use whatever method(s) to create a secure repair. The deltoid was securely reattached to the acromion with the deltoid fascia repaired down the split.
Intervention Type
Procedure
Intervention Name(s)
Arthroscopic acromioplasty with mini-open repair
Other Intervention Name(s)
Mini-open repair, Scope mini-open
Intervention Description
A standard arthroscopic gleno-humeral arthroscopy was performed followed by an arthroscopic acromioplasty. Three standard arthroscopic portals were used. The lateral portal was centered in line with the cuff tear, and incorporated into the mini-open incision. Initially, a partial bursectomy was performed to improve visualization. The inferior surface of the anterior acromion and the coracoacromial ligament were removed. Following the arthroscopic acromioplasty, a 3-4cm lateral incision was performed in the area of the lateral portal. The deltoid muscle was split longitudinally to expose the tear in the rotator cuff. The tear was repaired in a similar manner to the open repair with tendon to tendon sutures, trans-osseous sutures and with suture anchors.
Primary Outcome Measure Information:
Title
Rotator Cuff Quality of Life Questionnaire (RC-QOL)
Time Frame
Baseline, 3, 6, 12, 24 months
Secondary Outcome Measure Information:
Title
American Shoulder and Elbow Surgeons Score
Time Frame
Baseline, 3, 6, 12, 24 months
Title
Shoulder Rating Questionnaire
Time Frame
Baseline, 3, 6, 12, 24 months
Title
Functional Shoulder Elevation Test
Time Frame
Baseline, 6, 12, 24 months
Title
Range of motion
Time Frame
Baseline, 3, 6, 12, 24 months
Title
Strength
Time Frame
Baseline, 3, 6, 12, 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with unremitting pain in the affected shoulder who have failed conservative treatment for at least 3 months Weakness of rotator cuff (MRC grades 4-, 4 or 4+) Positive diagnostic imaging on the affected shoulder indicating a full-thickness rotator cuff tear which may include arthrogram, ultrasound or MRI Age > 18 years English speaking Exclusion Criteria: A massive rotator cuff tear as demonstrated by Grade 3 or less muscle strength on testing internal and external rotation of the affected shoulder Previous surgery to the affected shoulder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Hollinshead, MD, FRCSC
Organizational Affiliation
University of Calgary Sport Medicine Centre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nicholas Mohtadi, MD, FRCSC
Organizational Affiliation
University of Calgary Sport Medicine Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Calgary Sport Medicine Centre
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 1N4
Country
Canada
Facility Name
Royal Columbian Hospital
City
New Westminster
State/Province
British Columbia
ZIP/Postal Code
V3L 3W7
Country
Canada
Facility Name
Fowler Kennedy Sport Medicine Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 3K7
Country
Canada
Facility Name
Sunnybrook and Women's College Health Sciences Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4Y 1H1
Country
Canada

12. IPD Sharing Statement

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A Randomized Clinical Trial Comparing Open to Mini-Open Rotator Cuff Repair for Full-Thickness Rotator Cuff Tears.

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