This trial is active, not recruiting.

Condition torn anterior cruciate ligament (knee)
Treatment acl surgery
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.

United States No locations recruiting
Other countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification efficacy study
Intervention model parallel assignment
Masking single blind (subject)
Primary purpose treatment

Primary Outcomes

Endpoints Measured at 6, 12, 18 months post op compared to pre-op
time frame: Unspecified

Eligibility Criteria

Male or female participants at least 19 years old.

Inclusion Criteria: Torn ACL amenable to surgery Exclusion Criteria:

Additional Information

Official title Randomized Clinical Trial to Assess the Clinical Effectiveness of a Measured Objective Tensioning in Hamstring ACL Reconstruction
Principal investigator J Leith, MD
Trial information was received from ClinicalTrials.gov and was last updated in April 2011.
Information provided to ClinicalTrials.gov by University of British Columbia.