A study comparing Propofol plus fentanyl and Dexmedetomidine for conscious sedation in sclerotherapy patients.
Phase 1
Completed
- Conditions
- Health Condition 1: D233- Other benign neoplasm of skin of other and unspecified parts of face
- Registration Number
- CTRI/2019/01/016885
- Lead Sponsor
- PGIMER CHANDIGARH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 70
Inclusion Criteria
ASA 1
-Age group of 2-12 years
-Scheduled to undergo Sclerotherapy in IR department
Exclusion Criteria
-Acute Respiratory tract infections
-Predicted difficult airway
-History of allergy to propofol, fentanyl or dexmedetomidine
-Patients on sedatives within two weeks prior to surgery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Efficacy of sedation based on intraoperative patient movement scoreTimepoint: Base Line, Before administering bolus, after bolus, Every 2.5 minutes till procedure is over.
- Secondary Outcome Measures
Name Time Method Effect on hemodynamics and respiratory depression Ã? Recovery time from sedation <br/ ><br>Ã? Postoperative Pain Score (Visual Analogue Score)Timepoint: Every 2.5 minutes for hemodynmics and resiration <br/ ><br>end of procedure for pain