I gel in paediatric cardiac surgery
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/12/060459
- Lead Sponsor
- Armed Forces Medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Children aged less than 18 years undergoing surgery for acyanotic congenital heart disease requiring CPB with Mallampatti scoring of Gd 1 & 2 and not having any F/S/O URTI in the last 14 days
Exclusion Criteria
All patients with difficult airway, history of previous cardiac surgery, patients utilizing preoperative extracorporeal life support, patients who underwent surgery without cardioplegic arrest, emergency surgery, a history of reactive airway disease or gastroesophageal reflux and, morbid obesity.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary objective was to determine the viability of I-Gel for induction and maintenance of anaesthesia in children undergoing surgery for acyanotic congenital heart disease with cardiopulmonary bypass. The secondary objective was to achieve smoother and faster extubation with lower doses of opioid utilisation and better hemodynamic control in children undergoing surgery for acyanotic congenital heart disease with cardiopulmonary bypass.Timepoint: Intraoperative and immediate postoperative period
- Secondary Outcome Measures
Name Time Method The secondary objective was to achieve smoother and faster extubation with lower doses of opioid utilisation and better hemodynamic control in children undergoing surgery for acyanotic congenital heart disease with cardiopulmonary bypass.Timepoint: immediate postoperative