Post operative pain management in laparoscopic surgeries
Phase 4
- Conditions
- Health Condition 1: - Health Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2022/05/042764
- Lead Sponsor
- SDMCMSH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing elective laparoscopic abdominal surgeries of duration 60-120 mins
ASA Physical status 1,2
Those who willing to participate
Exclusion Criteria
1. Patient refusal.
2. Patients with ASA III and IV.
3. Patients with BMI < 18 kg/m2 and > 35 kg/m2.
4. Local infection at the site of block.
5. Allergy to study medications.
6.Chronic use of pain medications.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To compare the duration of analgesic effect by addition of dexamethasone and clonidine with ropivacaine in sub costal TAP block <br/ ><br>2. To determine VAS scores in first 24 h.Timepoint: 24 hrs
- Secondary Outcome Measures
Name Time Method To assess incidence of nausea or vomiting or other side effects, if any.Timepoint: 24 hrs