Pain relief in paediatric patients undergoing heart surgery via midline chest incision by two different blocks
Not Applicable
Completed
- Conditions
- Health Condition 1: I52- Other heart disorders in diseasesclassified elsewhere
- Registration Number
- CTRI/2021/11/038215
- Lead Sponsor
- Department of Cardiac Anaesthesia All India Institute of Medical Sciences New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 84
Inclusion Criteria
All elective cardiac surgeries in paediatric patients with acyanotic heart disease of age groups 6 months to 10 years, either sex and ASA 1 and 2 shall be included in the study; all these patients shall be candidates for fast tracking and extubation within 6 hours postoperatively i.e. procedures amenable for early extubation shall be included.
Exclusion Criteria
Emergency surgeries, redo surgeries, preoperative inotropic support, abnormal coagulation profile, preoperative ejection fraction <35%, low-cardiac-output syndrome, recurrent ventricular arrhythmias, allergic to the amide type of local anaesthetics (LA)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the efficacy of MICB and compare it with ESPB in paediatric cardiac surgical patients for post-sternotomy pain relief based on Modified Objective Pain Scores (MOPS) and rescue fentanyl consumptionTimepoint: At the time of extubation (0 hour), 1 hr., 2 hr., 4 hr., 6 hr., 8 hr., 10 hr., 12 hr.
- Secondary Outcome Measures
Name Time Method 1.Duration of analgesia and time to first dose of rescue analgesia <br/ ><br>2.Amount of opioid usage <br/ ><br>3.Duration of ICU and hospital stay <br/ ><br>4.Fast tracking and early extubation <br/ ><br>5.Ease of administering the block <br/ ><br>Timepoint: From the time of administering the block till discharge from ICU and hospital