Pain relief after operation by medication through tube placed beneath the skin in cardiac surgical patients
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/07/044245
- Lead Sponsor
- SNagaswetha
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. age groups 18-65 years of either sex 2. category 1 or 2 under CARE score (Cardiac Anaesthesia Risk Evaluation score) are included in the study viz. coronary artery disease with TVD and normal LV function, all valve replacement surgeries, ASD and VSD closure
Exclusion Criteria
1. emergency surgery 2. Redo surgeries 3. Preoperative inotropic support 4. preoperative poor left ventricular function (EF <40%) 5. clinically significant kidney or liver disease 6. COPD patients, uncontrolled DM 7. morbidly obese patients 8. Low cardiac output syndrome 9. patients allergic to local anaesthetics 10. preexisting coagulopathy 11. postoperative hemodynamic instability 12. If surgeon refuses
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the efficacy of ropivacaine infiltration by pre-sternal multi-orifice catheter for post-sternotomy pain relief in adult patients undergoing cardiac surgery based on Visual Analog Score (VAS) and rescue analgesic consumption.Timepoint: Visual analog scale assessment for 48hours
- Secondary Outcome Measures
Name Time Method Time to extubation â?¢ Postoperative respiratory parameters â?¢ Length of ICU stay â?¢ Incidence of wound infectionTimepoint: 171