Comparison of Dexmedetomidine as bolus or low â?? dose infusion to prevent postoperative agitation.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- AGE 2-12 YEARSHealth Condition 2: N398- Other specified disorders of urinary system
- Registration Number
- CTRI/2018/10/016088
- Lead Sponsor
- ONE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 48
Inclusion Criteria
Patients of ASA physical status Iâ??II, aged 2â??10 years of either sex with + 20% of ideal body weight, would be enrolled in this prospective, randomized, double blind study.
Exclusion Criteria
Patients with history of developmental delay, cardiac disorders, psychological disorders, epilepsy and allergy to study medications would be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To see emergence agitation by using PAEDS scale,pain by using OPS score and sedation by using RSS score.Timepoint: Postoperatively for one hour
- Secondary Outcome Measures
Name Time Method DRUG MORE EFFECTIVE FOR PREVENTION OF EMERGENCE AGITATION WITH BOLUS OR LOW DOSE INFUSION OF DEXMEDETOMIDINETimepoint: ONE YEAR