Comparing pain relief with continuous pain killer infusion for 24 hours given through tubes placed in abdominal wall and continuous pain killer infusion given through tube placed in lower back region following abdominal surgery
Phase 3
- Conditions
- Health Condition 1: null- All patients more than 18 years planned for elective abdominal surgery will be included
- Registration Number
- CTRI/2018/08/015412
- Lead Sponsor
- JIPMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients more than 18 years
Elective Open abdominal surgeries
American society of anesthesiologists (ASA) I, II and III.
Exclusion Criteria
Allergy to local anesthetist
Pregnancy
Patients on anti-coagulants
Patients on Pre-op opiods usage
Patients who do not comprehend VAS
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain relief by Visual Analogue Scale Score( Scale 0-10)Timepoint: 6 hours, 12 hours and 24 hours post op.
- Secondary Outcome Measures
Name Time Method Total leukocyte count, Interleukin-6, C- reactive protein measurementTimepoint: preoperative, immediate post op and 24 hours post operative period