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HEPMET-1: Evaluate the Feasibility, Mental Sideeffects and the Efficacy of Hepatitis C Treatment in a MMT Group.

Primary Purpose

Opiate Dependence, Hepatitis

Status
Completed
Phase
Phase 3
Locations
Norway
Study Type
Interventional
Intervention
Ribavirin
Pegylated Interferon
Sponsored by
Sorlandet Hospital HF
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opiate Dependence focused on measuring Chronical Hepatitis C treatment, Methadone Maintenance Treatment, Pegylated Interferon and Ribavirin, 14 weeks treatment, Genotype 2 and 3

Eligibility Criteria

25 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Serologic evidence of hepatitis C infection, genotype 2 and 3 Normal or elevated serum ALT activity In MMT-programme and with at least 6 months with satisfactory drug abuse control. That means no iv injections and no or minimal use of drugs. Male and female patients Exclusion Criteria: Women with ongoing pregnancy or breast feeding Untreated serious psychiatric disorders, particularly depression. Serious drug abuse or alcohol abuse last 6 months Intravenous drug abuse last 6 months Hepatitis A, B or HIV infection HCV genotype 1, 4, 5 and 6 Leucocytes < 3000 cells/mm3 at screening (neutrophil count <1500 cells/mm3) Platelet count < 80 000 cells/mm3 at screening Hb <11 g/dL in women or <12 g/dL in men at screening Documented or presumed coronary artery disease or cerebrovascular disease Thyroid dysfunction not adequately controlled Epilepsy Malignant disease

Sites / Locations

  • Soerlandet Hospital HF
  • Addiction Unit, Sorlandet Hospital

Outcomes

Primary Outcome Measures

- Percent of patients with sustained virological response, defined as undetectable HCV RNA 24 weeks after end of treatment

Secondary Outcome Measures

Retention in treatment, compliance, psychological distress, measures of quality of life, perceived drug use control and urine toxicology

Full Information

First Posted
September 6, 2005
Last Updated
March 26, 2008
Sponsor
Sorlandet Hospital HF
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1. Study Identification

Unique Protocol Identification Number
NCT00147784
Brief Title
HEPMET-1: Evaluate the Feasibility, Mental Sideeffects and the Efficacy of Hepatitis C Treatment in a MMT Group.
Official Title
HEPMET-1: Evaluate the Feasibility, Mental Sideeffects and the Efficacy of Hepatitis C Treatment in a Methadone Maintenance Treated (MMT) Opioid Addicted Group.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2008
Overall Recruitment Status
Completed
Study Start Date
March 2006 (undefined)
Primary Completion Date
June 2007 (Actual)
Study Completion Date
January 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Sorlandet Hospital HF

4. Oversight

5. Study Description

Brief Summary
To evaluate if weekly psychological follow-up make opioid dependent patients in MMT able to accomplish 14 weeks treatment with Peginterferon alfa-2a (PEG-INF) and ribavirin to the same extent than non-opioid dependents. To determine the efficacy of this anti-HCV treatment
Detailed Description
Chronic infection with the hepatitis C virus (HCV) is a health problem worldwide. In Norway, there are about 3000 patients participating in Methadone Maintenance Treatment(MMT) programs. A prevalence study at the MMT treatment unit in Kristiansand, showed that more than 90 % of 177 patients have been infected with hepatitis C. A major problem with anti-HCV treatment for this group is the lack of compliance and retention in treatment. Further, due to the high incidence of psychological disorders in opioid dependent patients, this may also complicate anti-HCV treatment. Drug addicted in MMT treatments programs may find themselves excluded from Hepatitis C treatment. Due to better treatment efficacy with the new PEG-INF's and encouraging reports from 14 weeks studies, it may be easier to motivate opioid dependents to fulfill treatment. Weekly psychological follow-up of these patients will further increase the possibility of opioid dependents in MMT to be able to complete anti-HCV treatment. The aim of this study is to focus on this patients situation, and strengthen their possibility to have a real opportunity to get treatment. We therefore wish to make a pilot study to investigate the feasibility, efficacy and psycological side-effects of the treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opiate Dependence, Hepatitis
Keywords
Chronical Hepatitis C treatment, Methadone Maintenance Treatment, Pegylated Interferon and Ribavirin, 14 weeks treatment, Genotype 2 and 3

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Ribavirin
Intervention Description
800 mg pr. os daily, 400 mg morning and 400 mg evening (200 mg/tbl.) for 14 weeks
Intervention Type
Drug
Intervention Name(s)
Pegylated Interferon
Intervention Description
180 mikrogram in 0,5 ml solution s.c. once a week for 14 weeks
Primary Outcome Measure Information:
Title
- Percent of patients with sustained virological response, defined as undetectable HCV RNA 24 weeks after end of treatment
Time Frame
24 weeks after end of treatment
Secondary Outcome Measure Information:
Title
Retention in treatment, compliance, psychological distress, measures of quality of life, perceived drug use control and urine toxicology
Time Frame
2, 4, 8, 14 and 24 weeks after study start

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Serologic evidence of hepatitis C infection, genotype 2 and 3 Normal or elevated serum ALT activity In MMT-programme and with at least 6 months with satisfactory drug abuse control. That means no iv injections and no or minimal use of drugs. Male and female patients Exclusion Criteria: Women with ongoing pregnancy or breast feeding Untreated serious psychiatric disorders, particularly depression. Serious drug abuse or alcohol abuse last 6 months Intravenous drug abuse last 6 months Hepatitis A, B or HIV infection HCV genotype 1, 4, 5 and 6 Leucocytes < 3000 cells/mm3 at screening (neutrophil count <1500 cells/mm3) Platelet count < 80 000 cells/mm3 at screening Hb <11 g/dL in women or <12 g/dL in men at screening Documented or presumed coronary artery disease or cerebrovascular disease Thyroid dysfunction not adequately controlled Epilepsy Malignant disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Oistein Kristensen, MD
Organizational Affiliation
Soerlandet Hospital HF
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Oistein Kristensen, MD
Organizational Affiliation
Addiction Unit, SSHF
Official's Role
Principal Investigator
Facility Information:
Facility Name
Soerlandet Hospital HF
City
Kristiansand
State/Province
Vest-Agder
ZIP/Postal Code
4604
Country
Norway
Facility Name
Addiction Unit, Sorlandet Hospital
City
Kristiansand
State/Province
Vest-Agder
ZIP/Postal Code
N-4604
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
19721480
Citation
Kristensen O, Sundoy A, Skeie K, Vederhus JK, Oye I, Opsal A, Rysstad O, Gallefoss F. [Short-term treatment of Hepatitis C in heroin-dependent patients]. Tidsskr Nor Laegeforen. 2009 Aug 27;129(16):1639-42. doi: 10.4045/tidsskr.09.33690. Norwegian.
Results Reference
derived

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HEPMET-1: Evaluate the Feasibility, Mental Sideeffects and the Efficacy of Hepatitis C Treatment in a MMT Group.

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