Regain of consciousness in dexmedetomidine-propofol vs ketamine-propofol in cardiac catheterisation in paediatric populatio
Phase 4
- Conditions
- Health Condition 1: PCS- Health Condition 2: 4- Measurement and MonitoringHealth Condition 3: 4- Measurement and Monitoring
- Registration Number
- CTRI/2022/01/039162
- Lead Sponsor
- PGIMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Both cyanotic and acyanotic heart disease children
2.Weight 5-20 kg, both genders
3.Paediatric patient undergoing sedation for cardiac catheterisation procedures including device closure and cath study with duration >30 min and <2 hours.
Exclusion Criteria
1.Patients already on mechanical ventilation
2.Patients requiring supplemental oxygen in pre op
3.Patients already on CPAP
4.Patients on ionotrops
5.Children with Downs syndrome
Study & Design
- Study Type
- PMS
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Regain of consciousness <br/ ><br>Timepoint: Minutes
- Secondary Outcome Measures
Name Time Method 1.Additional propofol requirement <br/ ><br>2.Respiratory depression <br/ ><br>3.Agitation <br/ ><br>4.Inotropic requirement <br/ ><br>5.Cardiac arrhythmia <br/ ><br>6.Intubation requirement <br/ ><br>Timepoint: Baseline, 5min, 10min, 15min,20min, 25min, 30min, 35min, 40min, 45min, 50min, 55min, 60min, 70min,80min,90min, 100min,120min