Comparative study done between effectiveness of two types of anaesthesia blocks for pain relief in children undergoing open heart surgery
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/06/053897
- Lead Sponsor
- Dr Siddharth M
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Children (3-7years) undergoing cardiac surgery
Exclusion Criteria
Thoracic wall defects
Age <3year or > 7years
Allergy to any local anaesthetic drug
Contraindication to blocks (deranged coagulation profile, coagulation/bleeding disorders)
Unwillingness to participate in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Ease of administration of block and duration of effectiveness of block <br/ ><br>Timepoint: At incision, at end of surgery, on arrival to ICU and at 4hrs, 8hrs, 12hrs, 16hrs, 20hrs, 24hrs <br/ ><br>
- Secondary Outcome Measures
Name Time Method eed for rescue analgesia in case of breakthrough painTimepoint: on arrival to ICU and at 4hrs, 8hrs, 12hrs, 16hrs, 20hrs, 24hrs <br/ ><br>