To test the effectiveness of two block in children for pain relief after heart surgeries.
Not Applicable
- Conditions
- Health Condition 1: Q211- Atrial septal defectHealth Condition 2: Q213- Tetralogy of FallotHealth Condition 3: Q210- Ventricular septal defect
- Registration Number
- CTRI/2023/05/052230
- Lead Sponsor
- Gandhi Medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) Age group 2-17 years of either sex.
2) Pediatric patients undergoing congenital cardiac correction (ASD,VSD and TOF etc) surgery with median sternotomy.
3) Patients of ASA grade II and III.
Exclusion Criteria
1) Parents of patients refusal/ consent not given.
2) History of developmental delay or mental retardation.
3)Known allergy to local anaesthetic.
4) Clinically significant liver or renal disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The effect of post-operative analgesia of erector spinal plane (ESP) block and pecto-intercostal fascial (PICF) block in pediatric cardiac surgeries using modified objective pain score(MOPS).Timepoint: When extubation criteria met, patient will be extubated and post-op pain assessment will be done at 0, 2, 4, 6, 8, 10 and 12 hrs.
- Secondary Outcome Measures
Name Time Method â??To observe intra operative and post operative opioid requirement and additional analgesic requirements. <br/ ><br>â??To observe the duration of analgesia in both groups. <br/ ><br>â??To observe adverse events, if any.Timepoint: At 0, 2, 4, 6, 8, 10 and 12 hrs.