Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Anhedonia
  • Cessation, Tobacco
  • Smoking (Tobacco) Addiction
  • Smoking Cessation
  • Smoking Tobacco
Type
Interventional
Phase
Phase 2
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Participants will be randomly assigned to receive either 300 or 450 mg of Bupropion XL.Masking: Triple (Participant, Care Provider, Outcomes Assessor)Masking Description: Participant will be unaware of which medication condition they have been assigned to, the care provider will not know which dose of medication they are distributing.Primary Purpose: Treatment

Participation Requirements

Age
Between 21 years and 65 years
Gender
Both males and females

Description

Participants will be randomly assigned to either receive 300 mg of BUP-XL or 450 mg of BUP-XL with an aim to quit smoking. They will take the medication for 8 weeks while simultaneously receiving counseling to set a quit date and stay motivated to quit. Medication will be administered for 4 weeks be...

Participants will be randomly assigned to either receive 300 mg of BUP-XL or 450 mg of BUP-XL with an aim to quit smoking. They will take the medication for 8 weeks while simultaneously receiving counseling to set a quit date and stay motivated to quit. Medication will be administered for 4 weeks before and 4 weeks after designated quit-date. Post-treatment follow-up appointment will be scheduled for 8, 16, and 26 weeks post treatment so assess commitment to quitting and overall success of the study.

Tracking Information

NCT #
NCT03326128
Collaborators
  • University of California, Los Angeles
  • University of California, San Diego
Investigators
Principal Investigator: Adam M Leventhal, PhD University of Southern California