Perioperative Analgesia in Palatoplasty Surgery.
Not Applicable
Recruiting
- Conditions
- Surgerycleft palate repair
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
ASA I or II
cleft palate repair
Exclusion Criteria
Children with hypersensitivity to lidocain, ketamine or dexmedetimodine
use of any other analgesic medication
children of ASA Physical Class III and IV; perioperative use of any analgesics
prolonged surgical procedure or extensive tissue dissection influencing the requirement of postoperative analgesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome was the perioperative analgesia of surgical site infiltration
- Secondary Outcome Measures
Name Time Method Children and Infants Postoperative Pain Scale (CHIPPS) ;Times to first cry (time taken for the child to cry after being handed to the mother in the recovery room);and time to feed (time taken for the child to tolerate milk feeds following the initial trial of milk feeds starting after 2 hours postoperative)
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the molecular mechanisms by which dexmedetomidine and ketamine enhance postoperative analgesia in cleft palate repair?
How does the combination of dexmedetomidine, ketamine, and lidocaine compare to standard-of-care analgesia in palatoplasty surgery?
Which biomarkers could predict patient response to surgical site infiltration with alpha-2 adrenergic agonists in cleft palate repair?
What are the potential adverse events associated with intraoperative use of dexmedetomidine and ketamine in pediatric patients?
Are there alternative adjuvant analgesics to ketamine and dexmedetomidine for improving pain management in cleft palate surgeries?