Yale Center for Clinical Investigations, Yale University
New Haven, Connecticut, 06519, United States
NCT Number: NCT02051309
Adult daily smokers motivated to quit smoking will be randomized to extended-release guanfacine (6mg/day) or placebo and will enroll in an 8-week treatment period combining medication with brief behavioral support. The investigators hypothesize that the active dose of guanfacine compared to placebo will increase rates of prolonged smoking abstinence at the end of the 8-week treatment phase.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 2
New Haven, Connecticut, 06519, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
6mg/day ER with 3-week lead-in period. Maintained at steady state throughout 8 week treatment phase. After treatment phase, given taper supply of medication. Follow up at 1 month, 2 months and 6 months.
Other names: Intuniv
Time frame: Week 3 to week 8 during 8-week treatment phase
Prolonged smoking abstinence defined as no relapse in week 3 to week 8, in participants with available outcome data during weeks 3 to 8.
Yale University
Other
Phase-II Clinical Trial Evaluating Guanfacine for Smoking Cessation
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