to compare dexmedetomidine and propofol for sedation during simple operative procedures.
Phase 2
- Conditions
- Health Condition 1: null- patients with impaired liver function
- Registration Number
- CTRI/2015/01/005465
- Lead Sponsor
- IDA NAWAZ
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
•Patients undergoing elective ERCP with impaired liver function (i.e. raised serum bilirubin ,SGOT or SGPT levels)
•Normal prothrombin time (PT) and international normalized ratio (INR)
•ASA grade II.
• Aged between 18 and 60 years.
•Those who are willing to give written informed consent
Exclusion Criteria
•ASA grade III or more.
•Patients with comorbid conditions such as HTN, DM or renal insufficiency.
•Patients having difficulty in communication (due to language problem or deafness).
•Patients with history of operative intervention in the past 72 hrs.
•Patients with the known allergy to these drugs and with a history of sulphite ,egg or soyabean allergy
•Pregnant patients.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method