Perioperative Analgesia in Palatoplasty Surgery.

Not Applicable

Recruiting

• Conditions: Surgery; cleft palate repair

• Registration Number: PACTR201606001686372

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-06-18
• Last Update Posted: 29 May 2023

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)