TO STUDY THE DIFFERENT DOSES OF INTRAVENOUS DEXMEDETOMIDINE ON BLOOD PRESSURE AND HEART RATE, DECREASE IN SUDDEN AWAKENING AT THE END OF SURGERY, INCIDENCE DIFFICULTIES IN BREATHING AND POST SURGERY SEDATION IN PAEDIATRIC PATIENTS FOLLOWING GENERAL ANAESTHESIA.
Phase 1
- Conditions
- Health Condition 1: null- Those undergoing surgeries under General anaesthesia
- Registration Number
- CTRI/2018/07/014700
- Lead Sponsor
- Rainbow Childrens Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients of ASA12 grade I or II.
2.Paediatric age group 3 months-12 years of either gender.
3.Patient scheduled to undergo elective surgical procedure under general anaesthesia.
Exclusion Criteria
1.Patients of ASA grade III or above.
2.Age less than 3 months and more than 12 years.
3.Patients physically dependent on narcotics.
4.Patients with history of drug allergy to Dexmedetomidine.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Heart rate, Systolic blood pressure, Diastolic blood pressure, mean arterail pressure, sedationTimepoint: Preinduction, After intubation, At dexmed infusion, At extubation, At 1, 5, 10 and 15 minutes after extubation <br/ ><br>
- Secondary Outcome Measures
Name Time Method Too much sedation, respiratory obstruction, laryngospasm, bronchospasmTimepoint: post operative