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Clinical Trials/NCT00971451
NCT00971451
Unknown
Not Applicable

Quadriceps Function Prior to Anterior Cruciate Ligament Reconstruction

University of Virginia1 site in 1 country50 target enrollmentNovember 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Rupture of Anterior Cruciate Ligament
Sponsor
University of Virginia
Enrollment
50
Locations
1
Primary Endpoint
Quadriceps muscle strength and inhibition using the quadriceps central activation ratio
Last Updated
15 years ago

Overview

Brief Summary

Patients who are diagnosed with an isolated tear of the anterior cruciate ligament and scheduled for arthroscopic reconstruction using bone-patellar tendon-bone autograft will be recruited to participate.

All subjects will be invited to participate in 2 weeks (2 supervised sessions per week) prior to their surgery. Each session will include supervised therapeutic exercises. Subjects will be randomly assigned to receive continuous transcutaneous electrical nerve stimulation (TENS) during each session or knee joint cryotherapy prior to each exercise session. The investigators will measure quadriceps function before and after this 2-week intervention (both sessions occur prior to reconstruction surgery). This study will also have a true control group that will not receive either exercise of modality intervention. The investigators will collect subjective and objective outcomes data at regularly scheduled post-operative visits.

Registry
clinicaltrials.gov
Start Date
November 2007
End Date
December 2011
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Complete ACL rupture

Exclusion Criteria

  • Persons who cannot tolerate knee joint TENS.
  • Persons who have a known allergy to cryotherapy
  • Patients who are pregnant or who plan on getting pregnant during the 12-month follow-up period.

Outcomes

Primary Outcomes

Quadriceps muscle strength and inhibition using the quadriceps central activation ratio

Time Frame: Day 15

Secondary Outcomes

  • Quadriceps H-reflex testing(Day 15)
  • International Knee Documentation Committee Subjective Knee Joint Evaluation(Day 15)
  • Visual Analog Scale(Day 15)
  • Tegner Activity Rating(Day 15)

Study Sites (1)

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