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Comparison of Three Methods for Anterior Cruciate Ligament Reconstruction

NCT00529958 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 330

Last updated 2024-12-11

Study results available
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Summary

The purpose of this randomized clinical trial is to determine the difference in quality of life outcome at two years, in patients undergoing an Anterior Cruciate Ligament (ACL) reconstruction procedure with either a patellar tendon, quadruple hamstring tendon or a double-bundle hamstring tendon autograft.

Conditions

  • Anterior Cruciate Ligament Rupture
  • Deficiency of Anterior Cruciate Ligament
  • Chronic Instability of Knee
  • Anterior Cruciate Ligament Injury

Interventions

PROCEDURE

Patellar Tendon

Patellar Tendon autograft

PROCEDURE

Hamstring Tendon

Quadruple Semitendinosus/Gracilis (Hamstring) Tendon Autograft

PROCEDURE

Double-Bundle

Double-Bundle Semitendinosus/Gracilis (Hamstring) Tendon Autograft

Sponsors & Collaborators

  • Workers' Compensation Board, Alberta

    collaborator OTHER

  • University of Calgary

    lead OTHER

Principal Investigators

  • Nicholas G Mohtadi, MD MSc FRCSC · University of Calgary Sport Medicine Centre

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
14 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2010-12-31
Completion
2023-09-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00529958 on ClinicalTrials.gov