To study and compare efficacy of 3 drug groups given as a nasal spray used to reduce anxiety and parenteral separation in children before surgery
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/05/066745
- Lead Sponsor
- Swami Rama Himalayan University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Children in the age group of 2-10 years
ASA grade 1 or 2
Either sex
Undergoing elective surgery procedures requiring GA with either Endotracheal Tube/Laryngeal mask airway for those patients in which consent has been given
Exclusion Criteria
children less than 2 and more than 10 years
ASA grade more than 2
emergency surgeries
known allergies to the above mentioned drugs
developmental delays/mental retardation
history of sedative/analgesic intake
history of congential heat disease/arrythmias
case of URTI
significant nasal discharge/obstruction
severe trauma of nose
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method parental separation anxiety based on a 4 point scoring system <br/ ><br>Timepoint: time interval taken to achieve a parental separation score of more than or equal to 2 as a desirable parameter
- Secondary Outcome Measures
Name Time Method mask acceptance <br/ ><br>intraop opiod use <br/ ><br>post op agitation <br/ ><br>post op emergence delirium <br/ ><br>post op nausea and vomitingTimepoint: intraop till end of surgery <br/ ><br>post op till 30 mins for agitation and 24 hours for rest