Varenicline + Prazosin for Heavy Drinking Smokers

The study comprises an 8-week double-blind, within-subjects, crossover design of varenicline
(up to 2mg per day) plus either prazosin (up to 8mg per day) (V+P) or placebo (V) with 20
heavy drinking smokers. Each medication phase is 3 weeks with a 2-week medication washout in
between. Participants are asked to make a practice quit attempt for 3 days the last week of
each medication phase.

This is an exploratory study to look at two primary aims:

1. Evaluate the effect of prazosin on sleep disturbance caused by varenicline in heavy
drinking smokers prior to quitting smoking.

Hypothesis: V+P will result in lower rates of vivid dreams and insomnia symptoms/sleep
discontinuity than V alone.

2. Evaluate the effect of prazosin on sleep disturbance caused by varenicline during
smoking cessation in heavy drinking smokers.

Hypothesis: V+P will result in lower rates of vivid dreams and insomnia symptoms/sleep
discontinuity than V alone We will also investigate the combined effects of prazosin and
varenicline on smoking behavior (i.e., smoking urge) and alcohol consumption (i.e., drinks
per drinking day) as exploratory aims.

Inclusion Criteria:

1. at least 18 years of age;

2. current smoker [quantity of ≥ cigarettes per smoking day, frequency of ≥3 times per
week, and urinary cotinine ≥2 on NicAlert dipstick;

3. at least 4 occasions of heavy drinking in the past 30 days [5 or 4 standard drinks
per occasion for males and females, respectively];

4. no history of severe alcohol withdrawal syndrome;

5. no new onset of psychiatric illness or psychotropic medications in last 90 days;

6. no severe psychiatric illness [schizophrenia, bipolar disorder] or PTSD;

7. no substance dependence other than nicotine, alcohol or marijuana;

8. no medical contraindications for varenicline or prazosin;

9. are willing to take medication and wear portable sleep monitoring devices;

10. no risk for sleep apnea syndrome;

11. able to read and write in English;

12. not interested in quitting smoking immediately.

Exclusion Criteria:

1. unable to complete the informed consent;

2. do not meet criteria for heavy drinking;

3. do not meet criteria for current smokers;

4. unable to read/understand English;

5. exhibit serious psychiatric illness (i.e. schizophrenia, bipolar disorder, severe
major depression, panic disorder, borderline personality disorder), organic mood or
mental disorders by history of psychological examination;

6. meet criteria for alcohol dependence in past 12 months that is clinically severe;

7. meet criteria for drug dependence in the last 12 months aside from marijuana,
nicotine and alcohol;

8. are seeking to quit smoking immediately;

9. report current psychosis or suicidality;

10. are a female of childbearing potential who is pregnant, nursing, or not practicing
effective contraception (oral, injectable, or implantable contraceptives,
intrauterine device, or barrier method with spermicide);

11. exhibit current, clinically significant physical disease or abnormality based on
medical history, physical examination, or routine laboratory evaluation including:

1. any unexplained elevations in liver enzymes (i.e. transaminases, bilirubin);

2. clinically significant, unstable cardiovascular disease/uncontrolled
hypertension;

3. hepatic or renal impairment;

4. severe obstructive pulmonary disease;

5. diabetes mellitus requiring insulin or certain oral medications (i.e.
sulfonylureas) and an A1C hemoglobin test score of >7 for participants not
prescribed these medications;

6. baseline systolic blood pressure higher than 150 mm Hg of diastolic blood
pressure higher than 95 mm Hg; (g) are scheduled for cataract surgery; (h) have
a diagnosis of narcolepsy;

12. have a history of cancer (except treated basal cell or squamous cell carcinoma of the
skin)

13. have a history of clinically significant allergic reactions;

14. have used any psychotropic drug in the past month, except individuals who are on a
stable dose of a Selective Serotonin Reuptake Inhibitor for at least two months;

15. intend to donate blood or blood products during the treatment phase of the study;

16. have a Body Mass Index (calculated as weight in kilograms divided by the square of
height in meters) less than 15 or greater than 28 or weight less than 45 kg.