Comparison between two doses of Dexmedetomidine through Epidural Infusion for Post-operative Pain Relief
Not Applicable
- Conditions
- Health Condition 1: M96-M96- Intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified
- Registration Number
- CTRI/2019/03/017895
- Lead Sponsor
- Sam Blessy Sheba
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients of both sex undergoing lower limb surgeries under Combined Spinal and Epidural Anaesthesia (CSEA) willing to be included in the study
Exclusion Criteria
1.Patients with Cardiac pathology
2.Hypertension
3.BMI <18 or >30 kg/m2
4.Known allergy to local anaesthetic infiltration
5.Chronic use of any other analgesics
6.American Society of Anaesthesiologists (ASA) III and above
7.Pregnant patients
8.Refusal for consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare analgesic efficacy in terms of Pain Scores in the first 24 hours postoperatively. <br/ ><br> <br/ ><br>Timepoint: To compare analgesic efficacy in terms of Pain Scores in the first 24 hours postoperatively. <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method â?¢To compare safety profile measured by sedation score and hemodynamic parameters up to 48 hours post operatively <br/ ><br>â?¢To compare pain scores in the next 24 hours, up to 48 hours postoperatively <br/ ><br> <br/ ><br>Timepoint: Postoperatively <br/ ><br>Postoperatively