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Clinical Trial Details — Status: Unknown status

Administrative data

NCT number NCT00750217
Other study ID # E-54/2007
Secondary ID
Status Unknown status
Phase Phase 4
First received September 9, 2008
Last updated September 9, 2008
Start date August 2008
Est. completion date May 2009

Study information

Verified date August 2008
Source Psychiatric University Hospital, Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Buprenorphine is an important alternative to methadone in the maintenance treatment of heroin addiction. Transfer from methadone to buprenorphine requires a reduction of daily methadone dosage below 30 mg to avoid withdrawal after the first buprenorphine intake. The study hypothesis states that the transfer from a daily methadone dosage between 60 mg and 100 mg to buprenorphine can be carried out without withdrawal using buprenorphine patches (35 micro grams per hour) within 12 to 48 hours after last methadone intake.


Recruitment information / eligibility

Status Unknown status
Enrollment 10
Est. completion date May 2009
Est. primary completion date February 2009
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Age between 18 and 60 years

- Methadone maintenance treatment for at least 3 months preceding the study

- Daily methadone dosage between 60mg amd 100mg

- Sufficient knowledge of German language

- Ability to give informed consent

Exclusion Criteria:

- Daily methadone dosage below 60mg amd over 100mg

- Prescribed use of benzodiazepines over 30 mg equivalent to diazepam

- Misuse or dependence of alcohol and/or GHB/GBL

- Pregnant or breast-feeding women

- Known intolerance of buprenorphine

- Somatic diseases interfering with the study plan

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Buprenorphine patch and sublingual tablets
Buprenorphine patch: 35 micro grams per hour 12 to 48 hours after last methadone intake. Buprenorphine sublingual tablets: 2mg 48 and 60 hours after last methadone intake; 8mg 72 and 84 hours after last methadone intake; 8mg 96, 102 and 109 hours after last methadone intake.

Locations

Country Name City State
Switzerland Psychiatric University Hospital Zurich

Sponsors (1)

Lead Sponsor Collaborator
Psychiatric University Hospital, Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Short Opiate Withdrawal Scale 14 days
Secondary Heroin use 60 days
See also
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Completed NCT00574067 - Buprenorphine for Prisoners Phase 3
Completed NCT00378079 - Methadone Maintenance for Prisoners Phase 3
Completed NCT01457872 - Malmö Treatment Referral and Intervention Study N/A
Active, not recruiting NCT04086459 - PET/MRI Study on the Neurological Mechanism of rTMS Treatment for Heroin Addiction N/A
Recruiting NCT01093248 - Methadone Maintenance Treatment Outcome Study in Taiwan N/A
Completed NCT02062736 - Observational Study to Assess the Adequacy of Methadone Dosage, in Heroin Addicted Patients in a MMT. N/A
Not yet recruiting NCT01668732 - Decision Making Deficit and DNA Methylation in Opioid Receptor Genes Among Community Heroin Addicts N/A