Cocktail Sedation Containing Propofol Versus Conventional Sedation for Endoscopic Retrograde Cholangiopancreatography (ERCP)
Disorders of Gallbladder, Biliary Tract and Pancreas
About this trial
This is an interventional treatment trial for Disorders of Gallbladder, Biliary Tract and Pancreas focused on measuring Cocktail sedation, ERCP
Eligibility Criteria
Inclusion Criteria:
- Patients scheduled for ERCP
Exclusion Criteria:
- Age under 18 years
- American Society of Anesthesiologists' (ASA) physical classification IV - V
- History of sulfite, egg or soy bean allergy
- Emergency need for ERCP
- Informed consent could not be obtained
Sites / Locations
- Gastroenterology Unit, King Chulalongkorn Memorial Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
conventional group
cocktail group
For induction, 25 mg of meperidine and 2.5 mg of midazolam were administered. To maintain conscious level of patient at moderate or deep level, 25 mg of meperidine and/or 2.5 mg of midazolam were administered as necessary.
For induction, 25 mg of meperidine and 2.5 mg of midazolam were administered. To maintain conscious level of patient at moderate or deep level, 1% propofol at the rate of 1 mg/kg/hr was administered. An additional 0.5 mg/kg bolus was administered as needed to achieve the designed conscious level.