A clinical trial to compare effectiveness of two regional anaesthesia techniques (Transverse thoracic muscle plane block and Erector spinae plane block)in controlling the pain after cardiac surgery
- Conditions
- Health Condition 1: R078- Other chest pain
- Registration Number
- CTRI/2024/08/072269
- Lead Sponsor
- Post Graduate Institute of Medical Education and Research, Chandigarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Patients with ASA status I and II undergoing elective cardiac procedure through
midline sternotomy, CABG where only venous graft is planned ,valve replacement surgery (MVR, AVR, DVR), septal defect surgery
(ASD, VSD)
patients who do not volunteer to participate, those who have Ejection fraction less than 35%, those with low cardiac output syndromes. on pre operative ionotropic support, wi9th reccurrent vascular anomalies. those who have allergy to local anaesthetics, those who have severe PAH. If its a reexplporation.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evaluate and compare the cumulative postoperative analgesic requirement (Fentanyl) within the initial 24 hours between two groups: one receiving Thoracic Transversus <br/ ><br>Thoracic Muscle Plane Block (TTMPB) , <br/ ><br>and the other receiving Erector Spinae Plane Block (ESPB)Timepoint: 24hrs
- Secondary Outcome Measures
Name Time Method To assess the time to first rescue analgesic (Fentanyl 0.5 mcg/kg) in each group (in <br/ ><br>min) to relate to the pain free time. <br/ ><br> <br/ ><br>To assess the analgesic efficacy of TTPMB & ESPB as measured by 11point NRS <br/ ><br>scores at 0,6,12 & 24 hrs. post extubation. <br/ ><br> <br/ ><br>To assess & compare the incidence of any complications or adverse events <br/ ><br>(hematoma, infection, pneumothorax, pericardial effusion etc.)Timepoint: 0,6,12,24 hrs