Status:
UNKNOWN
Efficacy of Oxycodone-propofol Combination Compared With a Fentanyl-propofol Combination on Conscious Sedation Effect and Early Cognitive Function During Therapeutic Endoscopic Retrograde Cholangio-pancreatography
Lead Sponsor:
Changhai Hospital
Collaborating Sponsors:
Wuhan University
Conditions:
Conscious Sedation During Endoscopic Retrograde Choledochopancreatography
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
To evaluate and compare the sedative effect and effects on early period cognitive function of a fentanyl-propofol Combination (FP) regimen with a oxycodone-propofol(OP) combination during the endoscop...
Detailed Description
One hundred patients undergoing ERCP were included in this study and randomly divided into two groups of 50 people each. The patients in group FP were given fentanyl infusion of 1ug/kg intravenously 5...
Eligibility Criteria
Inclusion
- ASA I-III
Exclusion
- cardiovascular disease
Key Trial Info
Start Date :
June 1 2018
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 1 2019
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT03755609
Start Date
June 1 2018
End Date
March 1 2019
Last Update
November 28 2018
Active Locations (1)
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1
Changhai Hospital
Shanghai, Shanghai Municipality, China, 200433