Comparison of respiratory problems during operation using either Propofol or Sevoflurane - Randomized trial
Not Applicable
- Conditions
- Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system
- Registration Number
- CTRI/2023/11/060122
- Lead Sponsor
- Armed Forces Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Children undergoing minor surgeries of duration less than 2 hours.
2. Patient should be eligible for LMA insertion.
3. Children with American Society of Anesthesiologist (ASA) status 1 - 2.
Exclusion Criteria
1. Pediatric patients with acute exacerbation of asthma.
2. Pediatric patients with congenital heart disease.
3. Pediatric patients with neurologic disorders.
4. Pediatric patients with full stomach.
5. Pediatric patients with hiatal heria.
6. Pediatric patients with known of predicted difficult airway.
7. Pediatric patients with facial or airway anomalies.
8. Pediatric patients with major abdominal or thoracic surgery.
9. Pediatric patients who had more than 3 attempts at LMA mask insertion.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare occurance of atleast one perioperative respiratory adverse event between <br/ ><br>TIVA with propofol & sevoflurane.Timepoint: Immediately till Half an hour post laryngeal mask airway removal
- Secondary Outcome Measures
Name Time Method The individual adverse event following removal of LMA mask.Timepoint: Immediately till Half an hour post laryngeal mask airway removal;The severity of airway hyper reactivity using the airway hyper reactivity score of <br/ ><br>Pappas et al. <br/ ><br>Timepoint: Immediately post laryngeal mask airway removal