Examination of children with glaucoma using a new modality for sedatio
Not Applicable
Completed
- Conditions
- Health Condition 1: H00-H59- Diseases of the eye and adnexa
- Registration Number
- CTRI/2019/01/017274
- Lead Sponsor
- Medical Education Cell Postgraduate Institute of Medical Education and Research Chandigarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1) Children with age of 6 months to years requiring Examination under sedation following surgery for pediatric glaucoma.
2) ASA (American Society of Anaesthesiologists) physical status I/II
Exclusion Criteria
Cardiorespiratory distress
bradycardia
upper respiratory tract infection
liver disease
seizures
acute medical condition
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Percentage of children having successful examination without requiring rescue sedative agent at 30minutes after intranasal dexmedetomidineTimepoint: 30 minutes after intranasal dexmedetomidine
- Secondary Outcome Measures
Name Time Method 1.Mean time of onset of adequate sedation score (Ramsayâ??s score) <br/ ><br>2.Sedation scores at 10 minutes, 20 minutes and 30 minutes after administration <br/ ><br>3.Need of rescue drug if no sedation after 30 minutes <br/ ><br>4. Surgeon satisfaction score for completion of procedure (IOP, Corneal diameter, ophthalmoscopy) <br/ ><br>5. Discharge time <br/ ><br>6. Adverse effects <br/ ><br>7. Parents satisfaction <br/ ><br>Timepoint: Sedation score will be assessed at 10, 20 and 30 minutes after administration of the drug.