A clinical trial to study the effect of dexmeditomidine in two different routes of administration in patients undergoing elective and emergency femur surgeries.
Phase 4
- Conditions
- Health Condition 1: null- Patients who have got femur bone frature
- Registration Number
- CTRI/2016/03/006757
- Lead Sponsor
- Ranjith Kumar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 78
Inclusion Criteria
1)Elective and emergency Femur bone surgeries,
2)American society of Anesthesiologist 1,2,3 physical status patients.
Exclusion Criteria
1)Coagulation disorders
2)Previous femoral bypass surgeries
3)Inflammation and infection over injection sites
4)Allergic to local anesthetics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Requirement of Perioperative analgesic agents <br/ ><br> <br/ ><br>Duration of analgesiaTimepoint: Requirement of perioperative analgesic agents at the time of skin incision of the surgery, requirement of analgesic agents intraoperatively and 24 hours post operatively.
- Secondary Outcome Measures
Name Time Method Perioperative hemodynamic outome <br/ ><br> <br/ ><br>Side effect profileTimepoint: 1.5 Years