Viewing Study NCT01505218


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Study NCT ID: NCT01505218
Status: COMPLETED
Last Update Posted: 2020-11-09
First Post: 2011-12-13
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Propofol Patient-controlled Sedation for Endoscopic Retrograde Cholangiopancreatography
Sponsor: University Hospital, Linkoeping
Organization:

Study Overview

Official Title: Patient-controlled Propofol Sedation for Endoscopic Retrograde Cholangiopancreatography
Status: COMPLETED
Status Verified Date: 2015-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: PER-projekt
Brief Summary: Propofol sedation with opioids is used for endoscopic retrograde cholangiopancreatography (ERCP). Combination of sedatives and opioids is associated with increased morbidity/mortality. Delivery of only propofol using a patient-controlled delivery system (patient-controlled sedation, PCS) could be an alternative for this purpose. Comparative studies with PCS for ERCP are few. Therefore, the main objective of this randomized controlled trial was to compare propofol PCS to sedation managed by nurse anaesthetists during ERCP.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: