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Nonalcoholic Steatohepatitis in HIV Mono-infection: Exploring Non-invasive Methods for Diagnosis and the Therapeutic Role of Vitamin E

Primary Purpose

HIV Mono Infection

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Vitamin E
Sponsored by
McGill University Health Centre/Research Institute of the McGill University Health Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Mono Infection

Eligibility Criteria

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

Inclusion Criteria:

  • Confirmed positive serology for HIV mono-infection and 18 years or older; valid Fibroscan/CAP;
  • Able to provide informed consent, signing forms available in French or English.
  • Fatty liver (CAP>237.8 dB/m) AND CK-18 levels > 246 U/L OR
  • Fatty liver (CAP>237.8 dB/m) AND CK-18 149 U/L + chronically elevated liver function tests (transaminases) + at least 1 metabolic risk factor (among diabetes, insulin resistance, dyslipidemia or overweight).

Exclusion Criteria:

  • Co-infection with HCV or HBV (presence of serum HCV-Ab or HbsAg); HCC, liver transplantation
  • Significant alcohol consumption, as per AASLD guidelines on NAFLD: "ongoing or recent alcohol consumption > 21 drinks on average per week in men and > 14 drinks on average per week in women"
  • Patients taking anticoagulants (warfarin, heparin)
  • Patients undergoing chemotherapy or radiotherapy for cancer
  • History of diagnosis of prostate cancer
  • Planning to become, suspected to be, pregnant or breastfeeding

Sites / Locations

  • Chronic Viral Illness Center at Royal Victoria Hospital in McGill university Health Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Vitamin E intervention

Arm Description

All study participants receive Vitamin E 800 IU once daily for 6 months

Outcomes

Primary Outcome Measures

Improvement of NASH diagnosed by non-invasive methods
Assessed by i) difference in AST and/or ALT
Improvement of NASH diagnosed by non-invasive methods
Assessed by ii) difference in Fibroscan/CAP measurements
Improvement of NASH diagnosed by non-invasive methods
Assessed by iii) difference in CK-18 levels

Secondary Outcome Measures

Change in metabolic markers
HOMA
Change in metabolic markers
Cholesterol or triglyceride levels
Change in metabolic markers
Weight and height will be combined to report BMI in kg/m^2

Full Information

First Posted
June 12, 2019
Last Updated
June 14, 2019
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
Collaborators
CIHR Canadian HIV Trials Network
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1. Study Identification

Unique Protocol Identification Number
NCT03988725
Brief Title
Nonalcoholic Steatohepatitis in HIV Mono-infection: Exploring Non-invasive Methods for Diagnosis and the Therapeutic Role of Vitamin E
Official Title
Nonalcoholic Steatohepatitis in HIV Mono-infection: Exploring Non-invasive Methods for Diagnosis and the Therapeutic Role of Vitamin E
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Completed
Study Start Date
November 11, 2014 (Actual)
Primary Completion Date
March 11, 2019 (Actual)
Study Completion Date
March 11, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
Collaborators
CIHR Canadian HIV Trials Network

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Effective combination antiretroviral therapy (cART) has resulted in a dramatic reduction in AIDS mortality. Over the last decade, the proportion of deaths caused by liver-related etiologies, including co-infection with hepatitis C (HCV) and hepatitis B (HBV) viruses, alcohol abuse, and fatty liver, has increased between 8 to 10 fold in the post-cART era while AIDS-related mortality has fallen more than 90-fold. HIV infection without viral hepatitis is also at risk for liver disease. Indeed, HIV mono-infected persons experience common conditions, such as obesity, diabetes and dyslipidemia, which are risk factors for non-alcoholic fatty liver disease (NAFLD). NAFLD is the most common liver disease in Canada. It is a fatty infiltration of the liver that is not evolutive per se, but it is the first histopathological step for non-alcoholic steatohepatitis (NASH), a progressive disease characterized by much inflammation leading to liver fibrosis and cirrhosis. NASH may be frequent in the setting of HIV mono-infection due to excess of metabolic risk factors, long-term cART, HIV itself and lipodystrophy. An early diagnosis of NASH is essential to establish a prognosis and initiate interventions to reduce progression of liver disease towards cirrhosis. Early diagnosis of NASH is critical for targeting metabolic and hepatologic interventions, which can impact on progression to cirrhosis and end-stage complications. Non-invasive tools for liver fibrosis and NASH, including Fibroscan/CAP and CK-18, are accurate and ideal for screening and serial monitoring. No study has specifically targeted the non-invasive diagnosis of NASH in HIV mono-infected patients. There has been no study about the use of CK-18 as a biomarker for NASH in the setting of HIV mono-infection. Furthermore, CAP has never been applied to this specific population. Finally, there is no data about the potential beneficial therapeutic effect of vitamin E on NASH associated to HIV infection. The investigators hypothesize that CK-18 and Fibroscan/CAP can be used as non-invasive tests to diagnose NASH in HIV mono-infected persons. Likewise, the investigators hypothesize that there will be a significant prevalence of NASH diagnosed by non-invasive tools among patients with HIV mono-infection. The investigators further hypothesize that a 6 months treatment trial with vitamin E supplementation will improve non-invasive diagnostic tests, and/or the metabolic and hepatic profile in HIV mono-infected patients with a non-invasive diagnosis of NASH.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Mono Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
27 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin E intervention
Arm Type
Experimental
Arm Description
All study participants receive Vitamin E 800 IU once daily for 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin E
Intervention Description
Vitamin E 800 IU once daily
Primary Outcome Measure Information:
Title
Improvement of NASH diagnosed by non-invasive methods
Description
Assessed by i) difference in AST and/or ALT
Time Frame
6 months
Title
Improvement of NASH diagnosed by non-invasive methods
Description
Assessed by ii) difference in Fibroscan/CAP measurements
Time Frame
6 months
Title
Improvement of NASH diagnosed by non-invasive methods
Description
Assessed by iii) difference in CK-18 levels
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Change in metabolic markers
Description
HOMA
Time Frame
6 months
Title
Change in metabolic markers
Description
Cholesterol or triglyceride levels
Time Frame
6 months
Title
Change in metabolic markers
Description
Weight and height will be combined to report BMI in kg/m^2
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed positive serology for HIV mono-infection and 18 years or older; valid Fibroscan/CAP; Able to provide informed consent, signing forms available in French or English. Fatty liver (CAP>237.8 dB/m) AND CK-18 levels > 246 U/L OR Fatty liver (CAP>237.8 dB/m) AND CK-18 149 U/L + chronically elevated liver function tests (transaminases) + at least 1 metabolic risk factor (among diabetes, insulin resistance, dyslipidemia or overweight). Exclusion Criteria: Co-infection with HCV or HBV (presence of serum HCV-Ab or HbsAg); HCC, liver transplantation Significant alcohol consumption, as per AASLD guidelines on NAFLD: "ongoing or recent alcohol consumption > 21 drinks on average per week in men and > 14 drinks on average per week in women" Patients taking anticoagulants (warfarin, heparin) Patients undergoing chemotherapy or radiotherapy for cancer History of diagnosis of prostate cancer Planning to become, suspected to be, pregnant or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Giada Sebastiani
Organizational Affiliation
Chronic Viral Illness Service, MUHC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chronic Viral Illness Center at Royal Victoria Hospital in McGill university Health Center
City
Montréal
State/Province
Quebec
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Nonalcoholic Steatohepatitis in HIV Mono-infection: Exploring Non-invasive Methods for Diagnosis and the Therapeutic Role of Vitamin E

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