Study of effect of intranasal ketamine on postoperative pain in childre
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/07/055681
- Lead Sponsor
- DR APOORVA S
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.CHILDREN IN THE AGE GROUP 5 TO 18 YEARS UNDERGOING SURGERY UNDER GENERAL ANAESTHESIA
2. CHILDREN IN ASA GRADE I TO II
Exclusion Criteria
CHILDREN WITH
1. ALLERGIC TO STUDY DRUG
2. ASA GRADE III OR > III
3. ABERRANT NASAL ANATOMY THAT PRECLUDES INTRANASAL MEDICATIONS.
4. PATIENTS UNDERGOING ANY NASAL SURGERY
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessement for postoperative pain after intranasal administration of ketamineTimepoint: At 15, 30,45,60 min, <br/ ><br>2,6, 12, 24 hours post operatively using modified Childrenâ??s Hospital of Eastern Ontario Pain Scale (CHEOPS) and Visual Analog Scale
- Secondary Outcome Measures
Name Time Method To determine the total amount of analgesicTimepoint: Anagesia required in first 24 hours post operatively