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Vitamin E Supplement in Patients With Cirrhosis and Acanthocytosis

Primary Purpose

Cirrhosis

Status
Completed
Phase
Phase 2
Locations
Switzerland
Study Type
Interventional
Intervention
Vitamin E supplement (tocofersolan)
Sponsored by
University Hospital, Geneva
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cirrhosis focused on measuring Cirrhotic patients

Eligibility Criteria

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

Inclusion Criteria:

  • Age > 18 years old
  • Cirrhosis (histology or, if not available, based on clinical, biological and radiological findings)
  • Total bilirubin > 60 µmol/ L
  • Anemia defined as hemoglobin < 120 g/L
  • Vitamin E deficiency as defined by plasma levels < 23 µmol/L

Exclusion Criteria:

  • Inability or unwillingness to give written consent
  • Parenteral nutrition
  • Co-medication with Orlistat, Colestipol, anticoagulants
  • Active alcohol consumption as assessed by urine analysis
  • Gastro-intestinal bleeding within the past 2 weeks
  • Gastric bypass
  • Moderate to severe renal failure as defined by creatinine clearance < 60 ml/min
  • Hypothyroidism as defined by TSH > 6 mU/L
  • Diagnosis of cancer upon inclusion in the study
  • Any other severe condition affecting interfering with the normal conduct of the study
  • Already participating in another clinical study

Sites / Locations

  • University Hospitals

Outcomes

Primary Outcome Measures

C/P (cholesterol to phospholipid) ratio of erythrocyte membrane before and after tocofersolan

Secondary Outcome Measures

percentage of acanthocytes in peripheral blood before and after tocofersolan
plasma levels of vit E before and after tocofersolan

Full Information

First Posted
October 19, 2011
Last Updated
March 17, 2014
Sponsor
University Hospital, Geneva
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1. Study Identification

Unique Protocol Identification Number
NCT01463735
Brief Title
Vitamin E Supplement in Patients With Cirrhosis and Acanthocytosis
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
November 2011 (undefined)
Primary Completion Date
May 2013 (Actual)
Study Completion Date
May 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Geneva

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Acanthocytes, also termed spur cell, are large erythrocytes covered with spike-like projections which are associated with severe hemolytic anemia. In advanced cirrhosis, acanthocytes may account for 20 to 30% of red blood cells. Up to 70% of cirrhotic patients display anemia and hemoglobin level may fall to below 5 gr/L in spur cell anemia. The true incidence of spur cells in cirrhosis is not known precisely but may avoisinate 45%, typically in patients with advanced cirrhosis.The presence of spur cells usually predicts lower survival rates. Vitamin E is an antioxidant compound that is a component of biological membrane that helps to maintain integrity of lipid bilayers. Vitamin E deficiency leads to erythrocyte hemolysis, which is improved by supplemental vitamin E. This study is an open label single arm phase II study in cirrhotic patients treated for 4 weeks with Tocofersolan (Vedrop), a water-soluble derivative of alpha-tocopherol, and thus an orally bio-available source of vitamin E. The aim of this study is to determine the effect of tocofersolan on red blood cell membranes lipid composition in adult patients with cirrhosis and vitamin E deficiency. Secondary endpoints are the effects of tocofersolan on anemia, hemolysis and acanthocytosis; on lipid peroxidation and oxidative stress; the safety of a 4 week treatment of 700 mg/day.
Detailed Description
Background: Cirrhosis may be complicated by the presence of ascites, portosystemic collaterals that may eventually bleed or give rise to hepatic encephalopathy. Laboratory findings in patients with cirrhosis includes alterations in synthetic function as well as an increase in serum bilirubin. Liver diseases are also associated with hematologic complications and altered red blood cells morphology. Up to 70% of cirrhotic patients display anemia and hemoglobin level may fall to below 5 gr/L in spur cell anemia. Thrombocytopenia, leucopenia and neutropenia are also common. In patients with cirrhosis, acanthocytes and echinocytes are reported. Acanthocytes, also termed spur cell, are large erythrocytes covered with spike-like projections which are associated with severe hemolytic anemia. In advanced cirrhosis, acanthocytes may account for 20 to 30% of red blood cells. The spiky morphology of acanthocytes results from an abnormal surface area to volume ratio and an altered membrane lipids composition. These changes in red blood cell membranes render the cell more prone to destruction and hemolysis. The true incidence of spur cells in cirrhosis is not known precisely but may avoisinate 45%, typically in patients with advanced cirrhosis.The presence of spur cells usually predicts lower survival rates. The liver is a very susceptible organ to oxidative-related cellular damage, and low antioxidants, such as vitamin E, in cirrhosis participate in cellular membrane alterations. Vitamin E is an antioxidant compound that is a component of biological membrane that helps to maintain integrity of lipid bilayers. Vitamin E deficiency leads to erythrocyte hemolysis, which is improved by supplemental vitamin E. Tocofersolan (Vedrop) is a water-soluble derivative of alpha-tocopherol, and thus an orally bio-available source of vitamin E. Vitamin E supplementation appears safe in liver diseases and provides histological benefit in NASH. Aim and endpoints I. To determine the effect of tocofersolan on red blood cell membranes lipid composition in adult patients with cirrhosis and vitamine E deficiency II. To determine the effect of vit E on anemia, hemolysis and acanthocytosis; on lipid peroxidation and oxidative stress; the safety of a 4 week treatment of 700 mg/day Duration: selection period: 1 week; active treatment: 4 weeks; follow-up period. 3 weeks. Evaluation time-points: baseline and after 4 weeks of treatment Methodology/Design: phase II pilot trial on 27 patients, single arm study

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhosis
Keywords
Cirrhotic patients

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
27 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin E supplement (tocofersolan)
Intervention Description
700 mg per day per os (i.e. 350 mg twice a day with meals)
Primary Outcome Measure Information:
Title
C/P (cholesterol to phospholipid) ratio of erythrocyte membrane before and after tocofersolan
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
percentage of acanthocytes in peripheral blood before and after tocofersolan
Time Frame
8 weeks
Title
plasma levels of vit E before and after tocofersolan
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years old Cirrhosis (histology or, if not available, based on clinical, biological and radiological findings) Total bilirubin > 60 µmol/ L Anemia defined as hemoglobin < 120 g/L Vitamin E deficiency as defined by plasma levels < 23 µmol/L Exclusion Criteria: Inability or unwillingness to give written consent Parenteral nutrition Co-medication with Orlistat, Colestipol, anticoagulants Active alcohol consumption as assessed by urine analysis Gastro-intestinal bleeding within the past 2 weeks Gastric bypass Moderate to severe renal failure as defined by creatinine clearance < 60 ml/min Hypothyroidism as defined by TSH > 6 mU/L Diagnosis of cancer upon inclusion in the study Any other severe condition affecting interfering with the normal conduct of the study Already participating in another clinical study
Facility Information:
Facility Name
University Hospitals
City
Geneva 14
ZIP/Postal Code
1211
Country
Switzerland

12. IPD Sharing Statement

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Vitamin E Supplement in Patients With Cirrhosis and Acanthocytosis

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