A study to assess pain after surgery to abdomen using pain injection given to abdome
Phase 2
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2024/01/061463
- Lead Sponsor
- Mysore Medical College and Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade 1 and 2 patients
Elective lower abdominal surgeries like inguinal hernia, incisional hernia, appendicectomy, under spinal anaesthesia
Exclusion Criteria
Patients refusal to the procedure
Any contraindications for regional anaesthesia techniques like infection at site of injection
Coagulation disorder
Use of opioids or alpha 2 agonist for sedation , pre medication or post operative analgesia
Incision extended to upper abdomen
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of analgesia after surgery at 2,4, 6,12 and 24 hours buy using VAS score <br/ ><br>Duration of post operative analgesiaTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Total rescue analgesia required in the first 24 hoursTimepoint: 24 hours