A prospective randomised trial of the use of tourniquet in total knee replacements
Not Applicable
Completed
- Conditions
- Surgery: Total knee replacement (TKR)SurgeryTotal knee replacement (TKR)
- Registration Number
- ISRCTN09327299
- Lead Sponsor
- Record Provided by the NHSTCT Register - 2007 Update - Department of Health
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 252
Inclusion Criteria
All patients undergoing total knee replacement at Stepping Hill Hospital under two named consultant surgeons
Exclusion Criteria
1. History of peripheral vascular disease with absent popliteal or distal pulses
2. Calcification of artery on x-ray of knee
3. Previous vascular surgery on side of operation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood loss and change in haemoglobin level day 2 post-operatively
- Secondary Outcome Measures
Name Time Method <br> 1. Range of movement six weeks post-op<br> 2. Post-operative wound problems<br> 3. Operative time<br> 4. Blood transfusion<br> 5. Complication rate<br>
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the molecular mechanisms of tourniquet use in total knee replacement (TKR) trials?
How does tourniquet application compare to standard-of-care techniques in TKR outcomes?
Are there biomarkers that predict optimal tourniquet use in TKR patients?
What adverse events are associated with tourniquet use in TKR and how are they managed?
What combination approaches or alternatives to tourniquets are being explored for TKR procedures?