The effectiveness of Dexmedtomidine and propofol during ERCP

Not Applicable

Recruiting

• Conditions: Failed moderate sedation during procedure; Sedation.; T88.52

• Registration Number: IRCT20190928044907N4
• Lead Sponsor: Babol University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 August 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Age18-65 years old
Absence of cardiovascular disease
ERCP candidate patients
Do not take sedatives
Absence of blood pressure
Absence of respiratory disease
Body Mass Index<30

Exclusion Criteria

History of drug abuse
Medical allergy
Kidney disease
Liver disease
Pregnancy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Heart Rate. Timepoint: Before starting the procedure, 5 minutes after starting, 15 minutes after starting the procedure and after finishing the work. Method of measurement: Number per minute.;O2 saturation. Timepoint: Before starting the procedure, 5 minutes after starting, 15 minutes after starting the procedure and after finishing the work. Method of measurement: Pulse oximeter.;Sedation. Timepoint: Before starting the procedure, 5 minutes after starting, 15 minutes after starting the procedure and after finishing the work. Method of measurement: Ramsay score.