Tourniquet vs. Short Time Tourniquet in Primary Robotic Assisted TKA
Completed · Not applicable
Conditions studied: Knee Arthropathy
In brief
The goal of this prospective, randomized study is to compare the outcomes of patients undergoing Robotic Arm-Assisted TKA (RA-TKA) with the intraoperative use of a tourniquet to those undergoing RA-TKA with a short tourniquet time.
Key facts
- Study ID
- NCT03942939
- Run by
- University of Louisville
- People needed
- 101
- Starts
- 2019-08-27
- Expected to finish
- 2020-07-15
- Last updated by the study team
- 2020-11-04
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient is over the age of 21
- Patient is scheduled to undergo a unilateral, cementless primary RA-TKA, secondary to osteoarthritis
- Surgical approach is subvastus approach
- Patient's BMI (body mass index) is less than 40 at time of surgery.
- Patient agrees to participate as a study subject and signs the Informed Consent and Research Authorization documents
- Patient is able to read and speak English
You may not qualify if…
- Patient is under the age of 21
- Patient's primary diagnosis is not osteoarthritis (e.g. post-traumatic arthritis)
- Patient is scheduled to undergo a bilateral TKA surgery
- Patient BMI is > 40
- Patient is unable to read and speak English
Where it is running
- Jewish Hospital — Louisville, Kentucky, United States
Full record on ClinicalTrials.gov
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