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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00310934
Other study ID # KarolinskaUH Regional 373/03
Secondary ID
Status Completed
Phase Phase 4
First received April 3, 2006
Last updated October 23, 2006
Start date August 2005
Est. completion date March 2006

Study information

Verified date March 2006
Source Karolinska University Hospital
Contact n/a
Is FDA regulated No
Health authority Sweden: Regional Ethical Review Board
Study type Interventional

Clinical Trial Summary

The objective of this study is to compare optimally given methadone maintenance treatment (MMT) for heroin dependence with a novel, sequential strategy, where patients are offered buprenorphine as first line treatment, allowed dose adjustments as needed, and switched to methadone if the maximal dose of buprenorphine is insufficient.


Description:

The objective of this study is to compare optimally given methadone maintenance treatment (MMT) for heroin dependence with a novel, sequential strategy (STEP), where patients are offered buprenorphine as first line treatment, allowed dose adjustments as needed, and switched to methadone if the maximal dose of buprenorphine is insufficient.

For this purpose, 96 subjects at two centers (Uppsala and Stockholm) are randomized to MMT or STEP and followed for 6 months. Retention in treatment is the primary outcome. Secondary outcomes in completers are proportion urine samples free of illicit opiates on app. twice weekly sampling, and problem severity as measured by a semistructured interview, the Addiction Severity Index (ASI) at baseline and after 3 and 6 months.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date March 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Heroin dependence according to DSM IV > 1year

- Age > 20 years

- Acceptance of the stated treatment principles.

Exclusion Criteria:

- Severe psychiatric illness such as dementia or psychosis compromising the patient’s ability to provide informed consent

- Other clinically significant psychiatric illness unless stable under treatment

- Severe medical condition such as advanced lung disease, unstable cardiovascular disease, severe liver disease

- Other clinically significant medical condition unless stable under treatment

- Treatment with anti-seizure drugs or disulfiram

- Pregnancy or intent to become pregnant within the next year

- Ongoing nursing

- Patients involuntarily discharged from a methadone or buprenorphine maintenance program within the last 3 months not eligible.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
methadone

buprenorphine / methadone sequence

Behavioral:
Relapse prevention

Contingency management


Locations

Country Name City State
Sweden Dept of Clinical Neuroscience, Karolinska Inst Stockholm

Sponsors (4)

Lead Sponsor Collaborator
Karolinska University Hospital Schering-Plough, Stockholm County Council, Sweden, Swedish National Drug Policy Coordinator

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Retention in treatment
Secondary Proportion urine samples free of illicit drugs
Secondary Problem severity as measured by Addiction Severity Index
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