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Clinical Trial Summary

The purpose of this study is to assess the risks of abuse, misuse and adverse events related to high dose buprenorphine. Approximately 1250 patients taking Subutex (Schering-Plough) or its Buprenorphine High Dose (BHD) generic (Arrow Laboratories) will participate in this study. Data will be collected using physician questionnaires and self evaluation patient questionnaires at the first visit and visits at 6 and 12 months.


Clinical Trial Description

Approximately 380 physicians will participate in this study. Patients will be enrolled in chronological order of consultations. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00723697
Study type Observational
Source Indivior Inc.
Contact
Status Completed
Phase
Start date May 2007
Completion date February 2010

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