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Clinical Trials/ACTRN12618001520224
ACTRN12618001520224Recruiting未知

Evaluation of post-operative graft laxity following Hamstring Tendon Autograft versus Quadriceps Tendon Autograft for Anterior Cruciate Ligament Reconstruction: A Randomised Controlled Trial

Mr Ross Radic0 sites112 target enrollmentStarted: September 11, 2018Last updated:

Trial Snapshot

Phase
未知
Status
Recruiting
Sponsor
Enrollment
112

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomised controlled trial
Primary Purpose
Treatment
Masking
Open (masking not used)

Eligibility Criteria

Ages
16 Years to 50 Years (—)
Sex
All

Inclusion Criteria

  • The individual is between the ages of 16 and 50 years.
  • The individual clinically qualifies for ACLR surgery based on clinical examination and MRI.
  • The individual has sustained the ACL tear within the last 12 months.
  • The individual is not currently being treated for a psychiatric disorder, senile dementia, Alzheimer’s disease, presence of alcohol/substance abuse.

Exclusion Criteria

  • The individual is unable or unwilling to sign the Patient Informed Consent, specific to this study, and approved by the Institutional Ethics Review Board.
  • The individual is unable or unwilling to follow the designated rehabilitation protocol.
  • The individual is classified as morbidly obese (>40 BMI).
  • The individual is skeletally immature.
  • The ACLR is combined with another ligament reconstruction or repair in the knee (multi- ligament knee reconstruction).
  • Revision ACLR procedures.

Investigators

Sponsor
Mr Ross Radic

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