Rotator Cuff Tear Clinical Trial
Official title:
Single Row Versus Double Row Fixation in Arthroscopic Cuff Repair; a Randomized Controlled Sutdy.
NCT number | NCT00508183 |
Other study ID # | OHREB2006862-01H |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2007 |
Est. completion date | July 2011 |
Verified date | March 2020 |
Source | Ottawa Hospital Research Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The study will identify if there is a difference of quality of life after surgery between two techniques used in surgery. The two different techniques are either the Single Row Fixation or the Double Row Fixation.
Status | Completed |
Enrollment | 90 |
Est. completion date | July 2011 |
Est. primary completion date | July 2011 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Patients who have failed standard non-surgical management of their rotator cuff tear, and who would benefit from a surgical repair of the cuff. - Imaging and intra-operative findings confirming a full thickness tear of the rotator cuff. Exclusion Criteria: - Characteristics of the cuff tear that render the cuff irrepairable. - Significant shoulder comorbidities - Previous surgery on affected shoulder - Patients with active workers compensation claims - Active joint or systemic infection - Significant muscle paralysis - Rotatorcuff tear arthropathy - Charcots arthropathy - Major medical illness - Unable to speak or read English - Psychiatric illness that precludes informed consent |
Country | Name | City | State |
---|---|---|---|
Canada | The Ottawa Hospital | Ottawa | Ontario |
Lead Sponsor | Collaborator |
---|---|
Ottawa Hospital Research Institute |
Canada,
Lapner PL, Sabri E, Rakhra K, McRae S, Leiter J, Bell K, Macdonald P. A multicenter randomized controlled trial comparing single-row with double-row fixation in arthroscopic rotator cuff repair. J Bone Joint Surg Am. 2012 Jul 18;94(14):1249-57. doi: 10.21 — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Western Ontario Rotator Cuff Index (WORC) | Do patients who undergo a repair of the rotator cuff with arthroscopic technique using double row fixation have increased disease specific quality of life (measured by WORC) then patients who undergo a repair with arthroscopic technique using single-row fixation? The WORC scale is from 0% to 100%, with a higher value being indicative of better disease specific quality of life. | 2 years | |
Secondary | Constant Score | Differences in outcome between the two groups as measured by the Constant score. The constant score ranges from 1 to 100 with a higher value indicative of better shoulder function. | 2 Year | |
Secondary | ASES Score | Determination of differences in outcome between the two groups as measured by the American Shoulder and Elbow Surgeons (ASES) score. The ASES score ranges from 0 to 100 with a higher number indicative of better function. | 2 Year | |
Secondary | Strength Test | Shoulder strength in forward elevation was measured in kg using a portable scale. | 2 Years | |
Secondary | Healing Rate | Percentage of Participants who had healed by 1 year post-surgery as measured using magnetic resonance imaging. If the tendons were in continuity with no evidence of full-thickness tearing, the repair was considered healed (intact). | 1 Year |
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