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
| Type | Name | Description |
|---|---|---|
| DRUG | Propofol VS. midazolam and fentanyl, endoscopies, liver diseases | 1. 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.