Trials / Withdrawn
WithdrawnNCT00748904
Rifaximin Versus Lactulose in Renal Failure
A Randomized Comparison of Rifaximin Versus Lactulose in Hospitalized Cirrhotic Patients With Progressive Renal Failure
- Status
- Withdrawn
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Weill Medical College of Cornell University · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate patients with cirrhosis of the liver and renal failure and determine if the administration of rifaximin as compared to lactulose is associated with less frequent and/or slower progression to severe hepatic encephalopathy. If one is associated with lower blood ammonia levels. And, if one is associated with lower breath hydrogen and methane levels.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Rifaximin | 400 mg orally |
| DRUG | Lactulose | 20 grams titrate to 2-3 bowel movements in one day |
Timeline
- Start date
- 2008-06-01
- Primary completion
- 2009-07-01
- Completion
- 2009-07-01
- First posted
- 2008-09-09
- Last updated
- 2022-02-08
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00748904. Inclusion in this directory is not an endorsement.