A clinical trial to study the comparative effects of two drugs dexmetedetomidine or fentanyl when added to ropivacaine for regional abdominal block
Not Applicable
- Conditions
- Health Condition 1: K352- Acute appendicitis with generalized peritonitisHealth Condition 2: K420- Umbilical hernia with obstruction,without gangrene
- Registration Number
- CTRI/2023/11/059384
- Lead Sponsor
- Gandhi Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. After obtaining approval from institutional Ethics Committee and informed written consent will be taken from all patients.
2. Patients of ASA grade 1&2.
3. Age group between16-50 years of both sex.
4. All patients undergoing for abdominal surgeries.
Exclusion Criteria
1. Patients refusal or not giving consent.
2. Patients with history of cardiac, respiratory, renal or hepatic failure.
3. Psychological disorders, local skin infections or disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To observe intra operative and post operative opioid requirement and additional analgesic requirements. <br/ ><br>To observe the duration of analgesia in all 3 groups. <br/ ><br>To observe adverse events if any for 2 hoursTimepoint: To observe intra operative and post operative opioid requirement and additional analgesic requirements. <br/ ><br>To observe the duration of analgesia in all 3 groups. <br/ ><br>To observe adverse events if any for 2 hours
- Secondary Outcome Measures
Name Time Method To assess the hemodynamic parameters & any complications for 2 hoursTimepoint: To assess the hemodynamic parameters & any complications for 2 hours