Varenicline for Nicotine Dependence Among Those With HIV/AIDS

Completed · Phase 3 · Has a placebo group

Conditions studied: Nicotine Dependence

In brief

Among people diagnosed with HIV/AIDS, the widespread use of highly active antiretroviral therapy (HAART) has greatly improved survival rates and changed the leading causes of death, from AIDS-related diseases to cardiovascular disease and lung cancer. Rates of tobacco use among individuals with HIV/AIDS are very high and varenicline may be particularly efficacious for treating nicotine dependence among individuals with HIV/AIDS. Through this trial, 310 smokers with HIV/AIDS will be randomized to varenicline plus 9 weeks of smoking cessation counseling or placebo plus 9 weeks of smoking cessation counseling. The investigators hypothesize that 1) varenicline and counseling will significantly increase end-of-treatment (week 12) and 24-week biochemically-confirmed abstinence, versus placebo and counseling; 2) quality of life will be rated higher in the varenicline and counseling group versus the placebo and counseling group, and there will be no significant differences between treatment arms in terms of the frequency of severe varenicline-related side effects; and 3) improved affect and reduced cognitive impairment will mediate the effect of varenicline therapy on quit rates.

Key facts

Study ID: NCT01710137
Run by: University of Pennsylvania
People needed: 179
Starts: 2012-10-01
Expected to finish: 2018-09-01
Last updated by the study team: 2019-09-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

18 years of age or older who self-report smoking at least 5 cigarettes (menthol and non-menthol) per day, on average.
Diagnosed with HIV infection and exhibiting viral load of < 1000 copies/mL and CD4+ counts of > 200 cells/mm3 within 6 months prior to enrollment.
Able to use varenicline safely, based on a medical evaluation including medical history and physical examination, and psychiatric evaluation.
Residing in the geographic area for at least 7 months.
Women of childbearing potential (based on medical history and physical exam) must consent to use a medically accepted method of birth control (e.g., condoms and spermicide, oral contraceptive, Depo-Provera injection, contraceptive patch, tubal ligation) or abstain from sexual intercourse during the time they are taking study medication and for at least one month after the medication period ends.
If current or past diagnosis of bipolar disorder (I, II, or NOS), eligible if:
No psychotic features
MADRS: total score < 8 (past 4 weeks), suicidal item score < 1 (past 4 weeks)
Y-MRS: total score < 8 (past 4 weeks), irritability, speech content, disruptive, or aggressive behavior items score < 3 (past 4 weeks)
No psychiatric hospitalization or Emergency Room visits for psychiatric issues in the past 6 months
No aggressive or violent acts or behavior in the past 6 months
Able to communicate fluently in English.
Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the combined consent/HIPAA form.

You may not qualify if…

Smoking Behavior
Current enrollment or plans to enroll in another smoking cessation program in the next 7 months.
Regular (daily) use of chewing tobacco, snuff, snus, cigars, cigarillos, or pipes.
Current use or plans to use nicotine substitutes (gum, patch, lozenge, e-cigarette) or smoking cessation treatments in the next 7 months.
Note: Once participants are found eligible for the study, they are told they should refrain from using any nicotine replacement therapy (NRT) for the duration of the study. If a subject reports an isolated (non-daily) instance of NRT use during the study, they may be permitted to continue.
Alcohol/Drug Exclusion Criteria
Current untreated and unstable diagnosis of substance abuse or dependence (eligible if past use and if receiving treatment and stable for >30 days).
Positive urine drug screen (for cocaine and/or methamphetamines) at the Intake Session.
Breath Alcohol Concentration (BrAC) assessment greater than or equal to 0.01 at the Intake Session.
Medication Exclusion Criteria
Current use or recent discontinuation (within last 14 days) of the following medications:
Other smoking cessation medications (e.g. Zyban, Wellbutrin, Wellbutrin SR, Chantix)
a. Note: Once participants are found eligible for the study, they are instructed to only use the smoking cessation medication provided to them by the study staff. If a subject reports an isolated (non-daily) instance of using a non-study smoking cessation medication, the study physician and PI will evaluate the situation and determine if it is safe for the subject to continue participation.
Anti-psychotic medications.
Medical Exclusion Criteria
Women who are pregnant, planning a pregnancy within the next 7 months, or lactating.
Current diagnosis of unstable and untreated major depression, as determined by self-report \& MINI (eligible if stable for >30 days).
Current or past diagnosis of psychotic disorder, as determined by self-report or MINI.
Any suicide risk score on MINI, current suicidal ideation on Columbia scale, or self-reported lifetime suicide attempt.
History of heart disease, stroke or MI, unstable angina, or tachycardia (if stable, requires Study Physician approval).
Uncontrolled hypertension (SBP >160 or DBP >100).
a. Note: If a participant presents with blood pressure greater than 160/100 at sessions occurring on Week 0 (Pre-Quit) or at any other point during the treatment period, they will not be provided with/able to continue on medication unless the study physician grants approval.
History of kidney or liver failure.
Abnormal ECG (unless approved by study physician).
Estimated creatinine clearance <50 mL/min, within 6 months prior to enrollment.

Where it is running

University of Pennsylvania — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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