Overview

Chantix & Bupropion for Smoking Cessation

Status:
Completed
Trial end date:
2008-07-01
Target enrollment:
0
Participant gender:
All
Summary
The overarching goal of this line of research is to increase smoking abstinence rates using a combination of existing pharmacotherapies. The aim of the current study is to assess the safety and compliance as well as obtain preliminary estimates of efficacy and effect on craving and nicotine withdrawal of combination therapy with bupropion SR and varenicline. We will compare the efficacy estimates in this study with historical smoking abstinence rates with varenicline. To accomplish our aims, we will enroll 38 cigarette smokers in an open-label, phase II clinical trial.
Phase:
Phase 3
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Mayo Clinic
Treatments:
Bupropion
Varenicline
Criteria
Inclusion Criteria:

- at least 18 years of age

- have smoked 10 or more cigarettes per day for at least 6 months

- are motivated to stop smoking.

Exclusion Criteria:

- an unstable medical condition

- unstable angina, myocardial infarction, or coronary angioplasty within the past 3
months or an untreated cardiac dysrhythmia

- personal history of seizures

- closed head trauma with any loss of consciousness or amnesia in the last 5 years

- ever history of closed head trauma with > 30 minutes of loss of consciousness or
amnesia or resulting in skull fracture or subdural hematoma/brain contusion

- a history or psychosis, bipolar disorder, bulimia or anorexia nervosa)

- have current depression as assessed by Center for Epidemiologic Studies Depression
(CES-D)

- have active substance abuse other than nicotine

- have used an investigational drug within the last 30 days

- are currently using a behavioral or pharmacologic tobacco treatment and unwilling or
unable to discontinue use

- use of bupropion or varenicline in the previous 3 months

- current (past 14 days) use of antipsychotic or antidepressant

- an allergy to bupropion or varenicline

- untreated hypertension or baseline systolic blood pressure > 180 or diastolic > 100

- have another member of their household already participating in this study.