Effects of Prednisolone and Pentoxifylline on the Regulation of Urea Synthesis in Alcoholic Hepatitis
This study is currently recruiting participants.
Verified October 2012 by University of Aarhus
Sponsor:
University of Aarhus
Information provided by (Responsible Party):
University of Aarhus
ClinicalTrials.gov Identifier:
NCT01245257
First received: November 15, 2010
Last updated: October 15, 2012
Last verified: October 2012
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Purpose
Loss of total mass of muscles (catabolism) is a serious clinical problem in patients with alcoholic hepatitis. The liver might play an important role in this stress-catabolism by increasing the production of urea during the inflammatory process.
The purpose of this study is to examine the regulation of urea synthesis in patients with alcoholic hepatitis and to study the effect of the anti-inflammatory drugs prednisolone and pentoxifylline on this regulation.
| Condition |
|---|
|
Alcoholic Hepatitis |
| Study Type: | Observational |
| Study Design: | Observational Model: Case-Crossover Time Perspective: Prospective |
| Official Title: | Effects of Prednisolone and Pentoxifylline on the Regulation of Urea Synthesis in Alcoholic Hepatitis |
Resource links provided by NLM:
Drug Information available for:
Prednisolone
Prednisolone acetate
Methylprednisolone acetate
Carbamide
Methylprednisolone
Carbamide peroxide
Prednisolone sodium phosphate
Prednisolone phosphate
Prednisolone sodium succinate
Methylprednisolone sodium succinate
Pentoxifylline
Hepatitis A Vaccines
U.S. FDA Resources
Further study details as provided by University of Aarhus:
Primary Outcome Measures:
- Functional Hepatic Nitrogen Clearance [ Time Frame: Before start of treatment ] [ Designated as safety issue: No ]
- Functional Hepatic Nitrogen Clearance [ Time Frame: Two weeks after start of treatment ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Clinical and biochemical measures of inflammation [ Time Frame: Before start of treatment ] [ Designated as safety issue: No ]
- Clinical and biochemical measures of inflammation [ Time Frame: Two weeks after start of treatment ] [ Designated as safety issue: No ]
Biospecimen Retention: Samples Without DNA
Serum, plasma, urine
| Estimated Enrollment: | 30 |
| Study Start Date: | November 2010 |
| Estimated Study Completion Date: | December 2014 |
| Groups/Cohorts |
|---|
|
Alcoholic Hepatitis
Patients with severe alcoholic hepatitis
|
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Study Population
Patients with alcoholic hepatitis admitted to hospital for treatment.
Criteria
Inclusion Criteria:
- Alcoholic hepatitis (alcohol intake (> 40g/day in 6 months), bilirubin > 150 μmol/l, Glasgow alcoholic hepatitis score ≥ 9)
Exclusion Criteria:
- Bacterial infections
- Other chronical inflammatory diseases
- Cancer
- Other catabolic diseases
- Treatment with prednisolone or pentoxifylline within the last 8 weeks
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01245257
Contacts
| Contact: Karen Louise Thomsen, MD | +45 89493897 | karethom@rm.dk |
Locations
| Denmark | |
| Department of Medicine V, Aarhus University Hospital | Recruiting |
| Aarhus, Denmark, 8000 | |
| Contact: Karen Louise Thomsen, MD +45 89493897 karethom@rm.dk | |
Sponsors and Collaborators
University of Aarhus
Investigators
| Principal Investigator: | Karen Louise Thomsen, MD | Aarhus University Hospital |
More Information
No publications provided
| Responsible Party: | University of Aarhus |
| ClinicalTrials.gov Identifier: | NCT01245257 History of Changes |
| Other Study ID Numbers: | FHNC-Alk-Hep |
| Study First Received: | November 15, 2010 |
| Last Updated: | October 15, 2012 |
| Health Authority: | Denmark: The Regional Committee on Biomedical Research Ethics |
Keywords provided by University of Aarhus:
|
Inflammation Urea Synthesis Catabolism Nitrogen balance |
Additional relevant MeSH terms:
|
Hepatitis, Alcoholic Hepatitis Hepatitis A Liver Diseases Digestive System Diseases Hepatitis, Viral, Human Virus Diseases Enterovirus Infections Picornaviridae Infections RNA Virus Infections Liver Diseases, Alcoholic Alcohol-Induced Disorders Alcohol-Related Disorders Substance-Related Disorders Methylprednisolone acetate |
Prednisolone acetate Prednisolone Methylprednisolone Methylprednisolone Hemisuccinate Prednisolone hemisuccinate Prednisolone phosphate Pentoxifylline Anti-Inflammatory Agents Therapeutic Uses Pharmacologic Actions Glucocorticoids Hormones Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs Antineoplastic Agents, Hormonal |
ClinicalTrials.gov processed this record on May 21, 2013