Sedation for Patients Undergoing Endoscopic Retrograde Cholangiopancreatography

• Status: Completed
• Trial end date: 2019-11-14
• Target enrollment: 0
• Participant gender: All

Summary

This study was performed to evaluate the role of BIS monitored sedation in reducing the dose of propofol and to know the effectiveness of pre-procedure administration of intravenous diclofenac sodium along with topical pharyngeal anesthesia in reducing the dose of propofol in patients undergoing endoscopic retrograde cholangiopancreatography.

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

Details

• Lead Sponsor: Institute of Liver and Biliary Sciences, India
• Treatments: Diclofenac; Lidocaine; Propofol

Criteria

Inclusion Criteria:

1. Age between 18-65 yrs

2. ASA I & II

Exclusion Criteria:

1. Age < 18 yrs & > 65 yrs

2. ASA III & IV patients

3. Chronic Liver Disease

4. Pregnant patients

5. Patients with a history of (H/O) Drug abuse

6. Patients refusing consent

7. H/o Acute kidney injury

8. H/o allergy to propofol / lidocaine/ NSAIDS

9. Post liver transplant patients

10. Patients with h/o egg allergy