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Clareo Health | Tourniquet vs. no Tourniquet During Total Knee Arthroplasty

Tourniquet vs. no Tourniquet During Total Knee Arthroplasty

NCT02907047·1 site·ClinicalTrials.gov

What this study is about

Take this into the appointment.

Saves the questions and what to expect into your notes, next to the visit they belong to.

Keep this study

Lead

Rothman Institute Orthopaedics

Age

18–any

Sex

ALL

Healthy volunteers

Not accepted

You may be eligible if

1. All unilateral primary knee arthroplasties performed by investigators participating in this study will be eligible for inclusion
2. Diagnosis of osteoarthritis

You may not be if

1. Revision surgery
2. Bilateral knee surgery
3. Age \<18 or \>80
4. BMI \>40
5. Baseline lower extremity strength less than 5/5
6. Vascular calcifications
7. History of chronic narcotic use, defined as more than 5mg of oxycodone q4 hours
8. Functionally limiting spine disease
9. Other functionally limiting lower extremity disorder (i.e. symptomatic ipsilateral hip disease)
10. Patients who cannot perform the baseline functional tests
11. Allergy/contraindication to protocol medications
12. Post-traumatic arthritis
13. Inflammatory arthritis
14. Pregnancy
15. Prisoners
16. Patients receiving care as part of a worker's compensable injury

The record

StatusCompleted

PhaseNo phase

Taking part—

StartedJun 2016

UpdatedJul 1, 2019

Conditions

Where1

Rothman Institute
Philadelphia, Pennsylvania, United States