Ondansetron, Alcohol Use, and Alcohol-Related Symptoms In HIV+ Persons



Status:Completed
Conditions:Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:18 - Any
Updated:3/10/2017
Start Date:December 2010
End Date:January 2017

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Ondansetron Pharmacotherapy for Hazardous Drinking in HIV+, African-American Women

The proposed randomized clinical trial will investigate a novel pharmacotherapy for
hazardous drinking, HIV-infected men and women, using the 5-HT3 antagonist ondansetron. The
investigators predict that participants who are treated with active doses of ondansetron
will reduce their drinking more and show better HIV treatment participation and progress
compared to participants who are treated with placebo. This study will provide important new
safety and efficacy results on drinking and HIV outcomes following alcohol pharmacotherapy
in HIV-infected persons.

Hazardous drinking is particularly harmful in HIV-infected persons. It impairs the immune
system, accelerates HIV disease progression, slows initiation of ART and decreases
adherence. Thus, the development of effective alcohol treatments for this clinical
population is particularly important. The investigators are proposing to investigate the
effectiveness of ondansetron pharmacotherapy for the treatment of hazardous alcohol use and
alcohol abuse/dependence among HIV-infected patients. Ondansetron, a 5-HT3 antagonist, will
be studied for several reasons: 1) evidence of effectiveness in persons who want to cut-down
or reduce their drinking and who are not abstinent at medication initiation; 2)
moderate-to-strong effects among early onset problem drinkers, a characteristic that is over
represented in our clinic patients; 3) a very mild side-effect profile, making it an ideal
pharmacotherapy candidate in patients who are often receiving multiple other medications
with significant side-effects; and 4) its primary indication is for treatment of nausea, a
common side-effect of antiretroviral (ARV) medications.

The proposed study is a placebo-controlled, randomized clinical trial of ondansetron for the
treatment of hazardous drinking and alcohol use disorders among HIV-infected patients
recruited from the Baltimore/Washington area. Participants will be genotyped for a
functional polymorphism of the serotonin transporter gene. They will be randomized to one of
three treatment groups: placebo, low dose ondansetron (0.2 mg bid) and moderate dose
ondansetron (0.8 mg bid). All subjects will undergo 16 weeks of pharmacotherapy in
combination with medication management, and will be followed for 3 and 6 months after
medication has ended.

Inclusion Criteria:

- Subjects will be at least 18 years old and HIV-infected

- All subjects will be actively drinking at hazardous levels (1) AUDIT score => 4 for
women or =>8 for men, or 2) => 2 binge drinking episodes/month, or 3) >7 drinks/week
for women or >14 drinks/week for men)

Exclusion Criteria:

- LFTs > 5 X normal

- Magnesium or potassium > 3 X normal

- Qtc => .460 and or a family history of LQT

- Inability to read and comprehend English

- Actively psychotic or other severe mental health symptoms that would prevent
appropriate participation

- Current enrollment in alcoholism treatment program

- Pregnancy; Ondansetron is currently a category B drug. While animal data have not
identified any harmful effects to mother or fetus, there have not been adequate human
controlled trials to recommend routine use in this population
We found this trial at
1
site
1800 Orleans St.
Baltimore, Maryland 21287
410-955-5000
Principal Investigator: Mary E McCaul, Ph.D.
Johns Hopkins Hospital Patients are the focus of everything we do at The Johns Hopkins...
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mi
from
Baltimore, MD
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