This study compares two drugs namely 0.5percent bupivacaine and 0.75 percent ropivacaine with an additive of dexmedetomidine used in transversus abdominis plane block for the duration of postoperative pain relief in patients undergoing lower abdominal surgeries under general anaesthesia
Phase 3
- Conditions
- Health Condition 1: G891- Acute pain, not elsewhere classifiedHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2024/07/070018
- Lead Sponsor
- Dr Harshitha Konanki
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients between ages of 18 and 65 years, ASA grade 1 and 2 undergoing lower abdominal surgeries under General Anaesthesia
Exclusion Criteria
ASA grade 3 and 4
Hypersensitivity to Local anaesthesia
patients with infection at the site of injection
patients who have coagulopathies
patients on systemic anticoagulant medications
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of postoperative analgesia after Transversus Abdominis Plane block in patients undergoing abdominal surgeries using 0.5 percent bupivacaine and dexmedetomidine compared with 0.75 percent ropivacaine and dexmedetomidineTimepoint: 2 hours, 4 hours, 9 hours, 18 hours, 24 hours
- Secondary Outcome Measures
Name Time Method Assessment of the effect of Transversus Abdominis Plane block on Perioperative hemodynamic status- Heart rate, Non-invasive Blood Pressure, SpO2Timepoint: 2 hours, 4 hours, 9 hours, 18 hours, 24 hours