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Pentoxifylline in Patients With Nonalcoholic Steatohepatitis

Primary Purpose

Nonalcoholic Steatohepatitis

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
pentoxifylline (PTX)
placebo
Sponsored by
Case Western Reserve University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nonalcoholic Steatohepatitis focused on measuring Fatty Liver, Nonalcoholic fatty liver disease (NALFD), NAFLD, Nonalcoholic steatohepatitis (NASH), NASH, pentoxifylline

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male and female patients ages 18 to 70 years.
  • Liver biopsy compatible with NASH, including presence of steatosis and necroinflammatory activity on liver biopsy done during the prior 6 months to study enrollment
  • Daily alcohol intake of <30 g for males and <15 g for females;
  • Appropriate exclusion of other liver diseases.
  • Patients with diabetes mellitus type 2 diagnosis as defined by a previous diagnosis of DM and current therapy with antidiabetic agents, or by fulfillment of 1997 American Diabetic Association (ADA) criteria, may be included if they fulfill the following criteria: (i) therapeutic regimen limited to specific oral agents including sulfonylureas (e.g. glipizide and glyburide) and/or biguanides (e.g. metformin); (ii) stable therapeutic regimen as defined by no changes in oral agents for at least 3 months; (iii) Hemoglobin A1C (HgbA1C) < 8.5 %.

Exclusion Criteria:

  • History of past excessive alcohol drinking (as defined above) for a period longer than 2 years at any time in the past 10 years.
  • Current consumption of alcohol >30 g daily for males and >15 g daily for females.
  • Positive testing for hepatitis B surface antigen, hepatitis C virus antibody, or ribonucleic acid (RNA) of hepatitis C virus of deoxyribonucleic acid (DNA) of hepatitis B virus.
  • Patients taking medications known to cause steatosis.
  • Other causes of liver disease suspected by history, family interview, or laboratory testing.
  • Patients with cirrhosis defined by stage 4 fibrosis on liver biopsy, or if the patient shows unequivocal clinical evidence of portal hypertension, such as thrombocytopenia, splenomegaly, or esophageal varices.
  • Patients taking medications of possible benefit in NASH within 3 months prior to the liver biopsy. These medications include Vitamin E, Betaine, S-adenosylmethionine (SAM-e), thiazolidinediones, and acarbose.
  • Patients with diabetes mellitus who are on Insulin therapy.
  • Patients with diabetes mellitus on therapy with thiazolidinediones or alpha-glucosidase inhibitors such as acarbose
  • Hypersensitivity to pentoxifylline or the methylxanthines (caffeine, theophylline, theobromine).
  • History of cerebral or retinal hemorrhage.
  • Other medical comorbidities (such as cardiac, central nervous system, renal, cancer) that would interfere with completion of the study.
  • Patients taking Theophylline or Coumadin because of potential drug-drug interactions with Pentoxifylline.
  • Pregnant or nursing women.

Sites / Locations

  • Louis Stokes VA Medical Center
  • Metrohealth Medical Center
  • Cleveland Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

Pentoxifylline (PTX) 400 mg by mouth (PO) three times daily (TID)

Placebo three times daily (TID)

Outcomes

Primary Outcome Measures

Histological Improvement of at Least 2 Points in NAFLD Activity Score (NAS) on Liver Biopsy After One Year.
The NAFLD Activity Score (NAS) grades NAFLD on liver biopsy based on the individual scoring of steatosis, inflammation and balloning. The NAS is assessed on a scale of 0 to 8 with higher scores indicating more severe disease and lower scores indicating less severe disease. NAS is obtained by adding steatosis(assessed on a scale of 0 to 3), inflammation (assessed on a scale of 0 to 3) and ballooning (assessed on a scale of 0 to 2).

Secondary Outcome Measures

Full Information

First Posted
December 26, 2007
Last Updated
August 5, 2013
Sponsor
Case Western Reserve University
Collaborators
American College of Gastroenterology
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1. Study Identification

Unique Protocol Identification Number
NCT00590161
Brief Title
Pentoxifylline in Patients With Nonalcoholic Steatohepatitis
Official Title
Treatment Efficacy of Pentoxifylline in Patients With Nonalcoholic Steatohepatitis: A Double-blind Randomized Placebo Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2013
Overall Recruitment Status
Completed
Study Start Date
December 2006 (undefined)
Primary Completion Date
July 2010 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Case Western Reserve University
Collaborators
American College of Gastroenterology

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
One third of the population in the United States has nonalcoholic fatty liver disease (NAFLD). Nonalcoholic steatohepatitis (NASH), the progressive form of NAFLD, can lead to cirrhosis.Currently, there is no proven therapy for patients with NASH. The investigators core hypothesis is that therapy of patients with NASH with pentoxifylline (PTX) for one year will result in improvement of biochemical parameters of liver disease and hepatic histology. The focus of this proposal is on the effectiveness of pentoxifylline (PTX) in improving laboratory and tissue parameters of liver disease, parameters of insulin-resistance, and levels of cytokines in patients with NASH.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nonalcoholic Steatohepatitis
Keywords
Fatty Liver, Nonalcoholic fatty liver disease (NALFD), NAFLD, Nonalcoholic steatohepatitis (NASH), NASH, pentoxifylline

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
55 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Pentoxifylline (PTX) 400 mg by mouth (PO) three times daily (TID)
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Placebo three times daily (TID)
Intervention Type
Drug
Intervention Name(s)
pentoxifylline (PTX)
Intervention Description
400 mg PO tid
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo tid
Primary Outcome Measure Information:
Title
Histological Improvement of at Least 2 Points in NAFLD Activity Score (NAS) on Liver Biopsy After One Year.
Description
The NAFLD Activity Score (NAS) grades NAFLD on liver biopsy based on the individual scoring of steatosis, inflammation and balloning. The NAS is assessed on a scale of 0 to 8 with higher scores indicating more severe disease and lower scores indicating less severe disease. NAS is obtained by adding steatosis(assessed on a scale of 0 to 3), inflammation (assessed on a scale of 0 to 3) and ballooning (assessed on a scale of 0 to 2).
Time Frame
1 year (Baseline liver biopsy done at study entry, and subsequent liver biopsy done after one year of therapy with pentoxifylline or placebo)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and female patients ages 18 to 70 years. Liver biopsy compatible with NASH, including presence of steatosis and necroinflammatory activity on liver biopsy done during the prior 6 months to study enrollment Daily alcohol intake of <30 g for males and <15 g for females; Appropriate exclusion of other liver diseases. Patients with diabetes mellitus type 2 diagnosis as defined by a previous diagnosis of DM and current therapy with antidiabetic agents, or by fulfillment of 1997 American Diabetic Association (ADA) criteria, may be included if they fulfill the following criteria: (i) therapeutic regimen limited to specific oral agents including sulfonylureas (e.g. glipizide and glyburide) and/or biguanides (e.g. metformin); (ii) stable therapeutic regimen as defined by no changes in oral agents for at least 3 months; (iii) Hemoglobin A1C (HgbA1C) < 8.5 %. Exclusion Criteria: History of past excessive alcohol drinking (as defined above) for a period longer than 2 years at any time in the past 10 years. Current consumption of alcohol >30 g daily for males and >15 g daily for females. Positive testing for hepatitis B surface antigen, hepatitis C virus antibody, or ribonucleic acid (RNA) of hepatitis C virus of deoxyribonucleic acid (DNA) of hepatitis B virus. Patients taking medications known to cause steatosis. Other causes of liver disease suspected by history, family interview, or laboratory testing. Patients with cirrhosis defined by stage 4 fibrosis on liver biopsy, or if the patient shows unequivocal clinical evidence of portal hypertension, such as thrombocytopenia, splenomegaly, or esophageal varices. Patients taking medications of possible benefit in NASH within 3 months prior to the liver biopsy. These medications include Vitamin E, Betaine, S-adenosylmethionine (SAM-e), thiazolidinediones, and acarbose. Patients with diabetes mellitus who are on Insulin therapy. Patients with diabetes mellitus on therapy with thiazolidinediones or alpha-glucosidase inhibitors such as acarbose Hypersensitivity to pentoxifylline or the methylxanthines (caffeine, theophylline, theobromine). History of cerebral or retinal hemorrhage. Other medical comorbidities (such as cardiac, central nervous system, renal, cancer) that would interfere with completion of the study. Patients taking Theophylline or Coumadin because of potential drug-drug interactions with Pentoxifylline. Pregnant or nursing women.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudia O Zein, MD, MSc
Organizational Affiliation
Case Western Reserve University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Louis Stokes VA Medical Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
Metrohealth Medical Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44109
Country
United States
Facility Name
Cleveland Clinic
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21748765
Citation
Zein CO, Yerian LM, Gogate P, Lopez R, Kirwan JP, Feldstein AE, McCullough AJ. Pentoxifylline improves nonalcoholic steatohepatitis: a randomized placebo-controlled trial. Hepatology. 2011 Nov;54(5):1610-9. doi: 10.1002/hep.24544. Epub 2011 Aug 24.
Results Reference
derived

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Pentoxifylline in Patients With Nonalcoholic Steatohepatitis

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