The purpose of this study is to correlate functional outcomes and perioperative complications
with tourniquet use during total knee arthroplasty.
Other: tourniquet inflated
Other: tourniquet not inflated
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT02907047
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
All unilateral primary knee arthroplasties performed by investigators participating in this study will be eligible for inclusion
Diagnosis of osteoarthritis
Bilateral knee surgery
Age <18 or >80
Baseline lower extremity strength less than 5/5
History of chronic narcotic use, defined as more than 5mg of oxycodone q4 hours
Functionally limiting spine disease
Other functionally limiting lower extremity disorder (i.e. symptomatic ipsilateral hip disease)
Patients who cannot perform the baseline functional tests
Allergy/contraindication to protocol medications
Patients receiving care as part of a worker's compensable injury
All locations for NCT02907047
United States (1)
Philadelphia, Pennsylvania, United States, 19148
View full eligibility
Tris trial is registered with FDA with number: NCT02907047. The sponsor of the trial is Rothman Institute Orthopaedics and it is looking for 0 volunteers for the current phase.
Official trial title:
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