Study for Comparison of Bloodloss, Range of motion and Functional Outcome in Total Knee Replacement with Tourniquet and without Tourniquet
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Patients with Osteoarthritis knee
- Registration Number
- CTRI/2018/05/014282
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Patients diagnosed with osteoarthritis scheduled for unilateral cemented TKA, either sex, aged <80 years
Exclusion Criteria
1. Severe obesity.
2. Previous operation in concerning knee.
3. Lack of informed consent.
4. Severe cardiovascular conditions.
5. Patients receiving general anaesthesia during surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
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 by which tourniquet use affects blood loss in total knee replacement for osteoarthritis patients?
How does tourniquet application compare to standard-of-care techniques in improving postoperative range of motion after total knee arthroplasty?
What biomarkers can predict functional outcomes in osteoarthritis patients undergoing total knee replacement with or without tourniquet use?
What are the potential adverse events associated with tourniquet use in total knee replacement and how are they managed clinically?
How do combination approaches involving tourniquet use and pharmacological interventions impact recovery in osteoarthritis-related total knee replacement?