Use of Graft Tensioner Device in ACL (Knee) Repair
This trial is active, not recruiting.
|Condition||torn anterior cruciate ligament (knee)|
|Sponsor||University of British Columbia|
|Start date||December 2010|
|End date||December 2011|
|Trial size||130 participants|
|Trial identifier||NCT00221273, C05-0302|
Compares tension of an ACL graft when using a commercial device vs. the tension of the graft applied by a physician during surgery.
|Endpoint classification||efficacy study|
|Intervention model||parallel assignment|
|Masking||single blind (subject)|
Endpoints Measured at 6, 12, 18 months post op compared to pre-op
time frame: Unspecified
Male or female participants at least 19 years old.
Inclusion Criteria: Torn ACL amenable to surgery Exclusion Criteria:
|Official title||Randomized Clinical Trial to Assess the Clinical Effectiveness of a Measured Objective Tensioning in Hamstring ACL Reconstruction|
|Principal investigator||J Leith, MD|
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