COMPARISION BETWEEN TWO BLOCKS FOR POST OPERATIVE ANALGESIA
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/06/053548
- Lead Sponsor
- GOVERNMENT MEDICAL COLLEGE, AMRITSAR
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients with American Society of Anaesthesiologists (ASA) Grade I or II 2. Patients with age 20-60 years 3. Patients undergoing thorasic and upper abdominal surgeries 4. Patients with no contraindications for peripheral area anaesthetic block
Exclusion Criteria
1.Patients with American Society of Anaesthesiologists (ASA) Grade III or IV 2. Patients with contraindications for local anaesthesia 3. Pre existing infection at the block site 4.Pre existing chronic pain or recognised dysfunction 5. Patient with abnormal blood coagulation 6. History of opioid abuse as this would stop the patient from taking part in postoperative quality of recovery and analgesia evaluation.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Time taken to perform the procedure ( Procedural time ) <br/ ><br>2. Duration of sensory blockade <br/ ><br>3. Time to first rescue analgesia <br/ ><br>4. Total dose of rescue analgesia in 24 hours.Timepoint: 1. Time taken to perform the procedure ( Procedural time ) <br/ ><br>2. Duration of sensory blockade <br/ ><br>3. Time to first rescue analgesia <br/ ><br>4. Total dose of rescue analgesia in 24 hours.
- Secondary Outcome Measures
Name Time Method 1.Post operative complications like Post operative nausea & vomiting(PONV) and post operative respiratory depression. <br/ ><br>2. Patientâ??s satisfaction scores <br/ ><br>3. Surgeon satisfaction scores <br/ ><br>4. Haemodynamic parametersTimepoint: Time from starting the procedure till 24 hours post surgery