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Clinical Trials/NCT02633410
NCT02633410
Completed
Not Applicable

Prospective Randomized Clinical Study Comparing Anteromedial Portal Versus Transtibial Technique for Femoral Tunnel Positioning in Anterior Cruciate Ligament Reconstruction With Hamstring Autograft

Panam Clinic0 sites96 target enrollmentJuly 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anterior Cruciate Ligament Reconstruction
Sponsor
Panam Clinic
Enrollment
96
Primary Endpoint
Anterior cruciate ligament quality of life
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The anteromedial (AM) portal technique was introduced to position the femoral tunnel in anterior cruciate ligament (ACL) reconstruction to more closely replicate the original footprint compared to the transtibial (TT) approach.1-5 Few randomized trials have evaluated differences in these techniques with respect to clinical outcomes. The purpose of this study was to determine if there are any differences in clinical outcome between the AM and TT approaches.

Detailed Description

The anteromedial (AM) portal technique was introduced to position the femoral tunnel in anterior cruciate ligament (ACL) reconstruction to more closely replicate the original footprint compared to the transtibial (TT) approach.1-5 Few randomized trials have evaluated differences in these techniques with respect to clinical outcomes. The purpose of this study was to determine if there are any differences in clinical outcome between the AM and TT approaches.

Registry
clinicaltrials.gov
Start Date
July 2007
End Date
July 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Panam Clinic
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • sustained a complete ACL tear and had no other ligament injuries requiring surgical intervention

Exclusion Criteria

  • concomitant collateral ligament tears
  • significant chondromalacia (based on diagnostic imaging)
  • previous lower limb surgery
  • significant injury to either lower limb requiring surgery
  • history of arthritis
  • were unable to comply with rehabilitation protocols or study follow-ups
  • were pregnant females or had other medical conditions which precluded participation.

Outcomes

Primary Outcomes

Anterior cruciate ligament quality of life

Time Frame: 24-months postoperative

Secondary Outcomes

  • Knee range of motion(24-months post-operative)
  • KT-1000(24-months post-operative)

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