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Pilot Study of Pentoxifylline for Hepatopulmonary Syndrome

Primary Purpose

Hepatopulmonary Syndrome

Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
pentoxifylline
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatopulmonary Syndrome focused on measuring hypoxemia, liver transplantation evaluation, cirrhosis

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient undergoing liver transplantation evaluation for cirrhosis
  • HPS (positive contrast echocardiography, hypoxemia, no other cause)
  • PaO2 < 65mmHg
  • ability and willingness to give informed consent

Exclusion Criteria:

  • Patients under the age of 19
  • active bacterial infections
  • known malignancy
  • intrinsic cardiopulmonary disease
  • known intolerance to pentoxifylline

Sites / Locations

  • University of Alabama at Birmingham

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

single

Arm Description

Outcomes

Primary Outcome Measures

change in arterial oxygenation (PaO2) and/or alveolar arterial oxygen gradient

Secondary Outcome Measures

adverse events and safety of pentoxifylline therapy

Full Information

First Posted
January 3, 2008
Last Updated
March 6, 2015
Sponsor
University of Alabama at Birmingham
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1. Study Identification

Unique Protocol Identification Number
NCT00593658
Brief Title
Pilot Study of Pentoxifylline for Hepatopulmonary Syndrome
Official Title
Open Label Single Arm Pilot Study of Pentoxifylline in Advanced Hepatopulmonary Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
January 2008
Overall Recruitment Status
Terminated
Why Stopped
Poor tolerability of drug and side effects
Study Start Date
June 2004 (undefined)
Primary Completion Date
October 2006 (Actual)
Study Completion Date
October 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Alabama at Birmingham

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The Hepatopulmonary syndrome (HPS) results from intrapulmonary microvascular dilatation that impairs arterial oxygenation in the setting of cirrhosis or portal hypertension. As many as 10-20% of cirrhotics being evaluated for orthotopic liver transplantation (OLT) have advanced HPS and mortality is greater in those with HPS than in those without HPS. Currently, OLT is the only effective treatment, although post-operative mortality in HPS is increased relative to cirrhotic patients without HPS, with a one-year survival of between 68-80 %. Therefore, an effective medical therapy for advanced HPS could improve both pre-operative and post-operative mortality. Recent work in experimental models of HPS has revealed that both nitric oxide synthase-derived nitric oxide and heme oxygenase-derived carbon monoxide cause intrapulmonary vasodilatation. These alterations appear to be driven in part by TNF-α modulation of pulmonary blood flow and intravascular monocyte accumulation. Pentoxifylline is a nonspecific phosphodiesterase inhibitor with inhibitory effects on TNF-α and has recently been shown to be beneficial in patients with severe alcoholic hepatitis where TNF-α overproduction contributes to liver injury. In experimental HPS, pentoxifylline administration also decreases the severity of oxygenation abnormalities. However, pentoxifylline therapy has been associated with dose limiting side effects in patients with liver disease and the tolerability of pentoxifylline in cirrhotic patients with advanced HPS is unknown. Therefore, this open label single arm clinical trial was designed to evaluate the efficacy and tolerability of 8 weeks of pentoxifylline in cirrhotic patients with advanced HPS being considered for OLT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatopulmonary Syndrome
Keywords
hypoxemia, liver transplantation evaluation, cirrhosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
single
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
pentoxifylline
Intervention Description
pentoxifylline extended release 800mg PO TID for 8 weeks
Primary Outcome Measure Information:
Title
change in arterial oxygenation (PaO2) and/or alveolar arterial oxygen gradient
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
adverse events and safety of pentoxifylline therapy
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient undergoing liver transplantation evaluation for cirrhosis HPS (positive contrast echocardiography, hypoxemia, no other cause) PaO2 < 65mmHg ability and willingness to give informed consent Exclusion Criteria: Patients under the age of 19 active bacterial infections known malignancy intrinsic cardiopulmonary disease known intolerance to pentoxifylline
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael B Fallon, MD
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18668653
Citation
Tanikella R, Philips GM, Faulk DK, Kawut SM, Fallon MB. Pilot study of pentoxifylline in hepatopulmonary syndrome. Liver Transpl. 2008 Aug;14(8):1199-203. doi: 10.1002/lt.21482.
Results Reference
derived

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Pilot Study of Pentoxifylline for Hepatopulmonary Syndrome

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