The comparison of propopfol alone versus propofol in combination with other medication for sedation in Endoscopic Ultrasonograph
Not Applicable
- Conditions
- Health Condition 1: null- ASA I,II and III patients scheduled for Endoscopic Ultrasound
- Registration Number
- CTRI/2016/11/007463
- Lead Sponsor
- ILBS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA physical status I,II and III patients scheduled for day care endoscopic ultrasongraphy
Exclusion Criteria
Refusal to participate in the study.
History of allergy to propofol.
Patients having cardiac disease, impaired renal function,uncontrolled hypertension, uncontrolled thyroid dysfunction, patients on antipsychotic medication
Pregnant and lactating mothers
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary end point of the study is successful completion of endoscopic procedure under sedationTimepoint: The primary end point of the study is successful completion of endoscopic procedure under sedation AT THE END OF THE PROCEDURE.
- Secondary Outcome Measures
Name Time Method time to discharge within 2 hoursTimepoint: every 15 mins upto 2hous after the procedure