A clinical trial to study the effect of prewarming on intraoperative blood loss and transfusion requirements in Total Hip Arthroplasty surgeries.
Phase 3
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: M879- Osteonecrosis, unspecified
- Registration Number
- CTRI/2021/04/033265
- Lead Sponsor
- AIIMS JODHPUR
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients scheduled for elective primary unilateral total hip arthroplasty under combined spinal epidural technique will be included in the study.
Exclusion Criteria
1. Patients planned for bilateral or revision total hip arthroplasty.
2. Patients with bleeding or coagulation disorders.
3. Patients on anticoagulants or antiplatelet drugs before surgery.
4. Patients with severe cardiovascular disorders.
5. Patients with thyroid disorders.
6. Patients with skin lesions or history of hypersensitivity to skin contact devices.
7. Patients with use of a transdermal medication patch.
8. Pre-existing preoperative hypothermia( <35.5degC) or hyperthermia( >37.5degC)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method