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Clinical Trials/NCT00221273
NCT00221273CompletedNot Applicable

Randomized Clinical Trial to Assess the Clinical Effectiveness of a Measured Objective Tensioning in Hamstring ACL Reconstruction

University of British Columbia0 sites130 target enrollmentStarted: December 1, 2010Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
130
Primary Endpoint
Endpoints Measured at 6, 12, 18 months post op compared to pre-op
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Compares tension of an ACL graft when using a commercial device vs. the tension of the graft applied by a physician during surgery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
19 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Torn ACL amenable to surgery

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Endpoints Measured at 6, 12, 18 months post op compared to pre-op

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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