Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
PHASE1
INTERVENTIONAL
1994-09-30
1999-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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TREATMENT
Interventions
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Bupropion
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
45 Years
ALL
No
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
VA Connecticut Healthcare System
FED
Yale University
OTHER
Responsible Party
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Principal Investigators
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Thomas R Kosten, M.D.
Role: PRINCIPAL_INVESTIGATOR
VA Connecticut Healthcare System
Locations
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VA Connecticut Healthcare System
New Haven, Connecticut, United States
Countries
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Other Identifiers
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P50-09250-1
Identifier Type: -
Identifier Source: secondary_id
NIDA-09250-1
Identifier Type: -
Identifier Source: org_study_id
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