Comparison of two drugs for pain relief after operation in patients of brain tumor excision using local anaesthesia
Not Applicable
- Registration Number
- CTRI/2024/04/065127
- Lead Sponsor
- Paras Hospitals Gurgaon
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1,2
Patients undergoing elective supratentorial craniotomy
GCS > 13-15
Exclusion Criteria
Known allergy to study drugs.
Refusal of consent.
Anticipated duration of surgery >6 hours.
Preoperative HR < 50/min.
Past history of craniotomy.
Pregnancy and lactation.
Patients unable to understand pain scores.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the post-operative analgesic requirement for first 24 hours after surgery.Timepoint: At the end of surgery and final evaluation after 1 year
- Secondary Outcome Measures
Name Time Method 1. To compare intraoperative analgesic requirements. <br/ ><br>2. To compare intraoperative hemodynamic parameters and their correlation with qnox values. <br/ ><br>3. To compare side-effects profile in all three groups. <br/ ><br>4. To compare pain scores using VAS values for first 24 hours in all three groups. <br/ ><br>Timepoint: During the surgery, at the end of the procedure and final evaluation after 1 year