Post operative agitation and hyperactivity in children can be reduced bydexmedetomidine and propofol-which is better
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/02/030983
- Lead Sponsor
- Dr S N Medical College Jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients aged 2 to 6 years of either gender of ASA PS I and II undergoing surgery under general anaesthesia with sevoflurane lasting less than 120min
Exclusion Criteria
1.Parentsâ?? refusal.
2.Patients posted for elective surgery under regional anaesthesia.
3.ASA III and IV
4.Patients with active URI.
5.Patient with history of previous psychiatric illness.
6.Patients with a history of developmental delay
7.Patients having congenital airway problems, cardiac disorders or syndromic babies
8.Patients having psychological disorders, epilepsy and allergy to the study medications
9.Surgeries lasting for more than 120 min
10.Surgeries requiring endotracheal tube insertion for securing the airway
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the incidence of emergence delirium in subjects receiving propofol or dexmedetomidine at the end of surgery with sevoflurane anaesthesia during a period of six months.Timepoint: 30 min
- Secondary Outcome Measures
Name Time Method To compare the hemodynamic parameters (HR, SBP, DBP, MAP, RR, SpO2, and ECG), sedation level, recovery time and post-operative pain between groups receiving propofol and dexmedetomidine.Timepoint: 30 min