Comparison of Different Ratio of Ketofol (6:1 vs. 4:1) for Sedation in Endoscopic Retrograde Cholangiopancreatography (ERCP)

• Status: Completed
• Trial end date: 2017-06-01
• Target enrollment: 0
• Participant gender: All

Summary

Study was aimed to compare the effect of ketofol between 6:1 and 4:1 ratio in patients who underwent ERCP

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Indonesia University
• Treatments: Ketamine; Propofol

Criteria

Inclusion Criteria:

• Having ERCP procedures using sedatives

• ASA (American Society of Anesthesiologist) physical status Class I to III

• Body mass index (BMI) of 18-30 kg/m2

• Willing to participate in the study

Exclusion Criteria:

• Patients with a history of allergic reaction to medications used in the study

• Patients with cardiovascular disease, uncontrolled hypertension, respiratory dysfunction

• Patients with unstable hemodynamic

• Patients with psychiatric medications

• Patients with probability of difficult intubation and ventilation Patients with kidney disorder Pregnant women