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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

Not Applicable
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
Inclusion Criteria

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)

Exclusion Criteria

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
NameTimeMethod
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
NameTimeMethod
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
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