407
Participants
Start Date
December 31, 2002
Primary Completion Date
January 31, 2005
Study Completion Date
September 30, 2009
Bupropion and NRT
All participants receive standard 12 week treatment of NRT, bupropion and five group counseling sessions. At week 11, subjects are randomly assigned to one of five treatment groups (1) Bupropion/Low Contact; (2) Placebo/Low Contact; (3) Bupropion/Relapse Prevention; (4) Placebo/Relapse Prevention; (5) No Further Treatment. Data is collected at Week 0, and at weeks 12, 24, 52, 64, and 104.
University California, San Francisco, San Francisco
National Institute on Drug Abuse (NIDA)
NIH