Clinical Trials Directory

Trials / Unknown

UnknownNCT00978978

Propofol Versus Midazolam and Fentanyl for Diagnostic and Screening Colonoscopy in Patients With Advanced Liver Disease

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Soroka University Medical Center · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Prospective, randomized-controlled trial (RCT) comparing the use of Propofol and traditional sedation (Midazolam and Fentanyl) for diagnostic and screening endoscopies in patients with liver diseases. The investigators' working hypothesis is that the use of propofol will be translated in a shorter recovery and discharge times with a higher patient satisfaction and a decrease in general complications in the context of patients with advanced liver disease.

Conditions

Interventions

TypeNameDescription
DRUGPropofol VS. midazolam and fentanyl, endoscopies, liver diseases1. Intervention group (Propofol): It will be administered as a monotherapy under direct gastroenterologists' 2. Control group (Midazolam with or without Fentanyl): Both drugs will be administered by the gastroenterologists

Timeline

Start date
2009-10-01
Primary completion
2010-08-01
First posted
2009-09-17
Last updated
2009-10-14

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00978978. Inclusion in this directory is not an endorsement.

Propofol Versus Midazolam and Fentanyl for Diagnostic and Screening Colonoscopy in Patients With Advanced Liver Disease (NCT00978978) · Clinical Trials Directory