Efficacy of children with cleft palate undergoing palatoplasty under General Anesthesia
Not Applicable
- Conditions
- Health Condition 1: Q378- Unspecified cleft palate with bilateral cleft lip
- Registration Number
- CTRI/2024/01/061203
- Lead Sponsor
- Department of Anaesthesiology and Intensive Care Unit
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade I and II patients.
Pediatric patients of age 1-5 years
All patients/ guardian giving written informed consent will be taken
All cleft palate patients
Exclusion Criteria
Patient/guardian not willing to participate in the study
Children who had an allergy to local anesthetics, any coagulation disorder, local infection
concomitant rhinoplasty,
any additional congenital anomalies,
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare effectiveness of sphenopalatine ganglion block vs palatal block on postoperative analgesia following palatoplasty using FLACC scoreTimepoint: 48 to 72hrs
- Secondary Outcome Measures
Name Time Method To compare the following criteria in both groups- <br/ ><br> need of rescue analgesia <br/ ><br>parental satisfaction using likert scale. <br/ ><br>Intraoperative hemodynamics <br/ ><br>Timepoint: 48 hrs