A comparison of dexmedetomidine combined with propofol for conscious sedation during endoscopic retrograde cholangiopancreatography(ERCP)

Phase 4

Recruiting

• Conditions: Although target controlled infusion(TCI) systems decrease the risk of respiratory during sedation with propofol, the risk persists.; Anaesthesiology - Anaesthetics

• Registration Number: ACTRN12612000964819
• Lead Sponsor: Dr Qianbo Chen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-09-07
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Adults without intubations undergoing ERCP

Exclusion Criteria

Any contraindication to sedation.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The sedation level was assessed by the Richmond alertness-sedation scale and bispectral index(BIS), and the demand for additional sedatives.[Intraoperative (less than three hours)]

Secondary Outcome Measures

Name	Time	Method
Heart rate, blood pressure, oxygen saturation, and respi-<br>ratory rate were recorded by cardiogram monitor (SK26-PC-9000C, China) before anesthesia, every 5 minutes during anesthesia, and 10 minutes after anesthesia, these will be recorded on the worksheet . The results will be compared between the two groups using variance analysis<br>by SPSS.[Intraoperative (less than three hours)]