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CompletedNCT03169244Updated Aug 26, 2020Results posted

Buproprion for Binge Drinking

A Phase 2 interventional study of Bupropion and Placebo Oral Tablet in Alcohol Abuse, sponsored by University of North Carolina, Chapel Hill. Completed at 1 site in United States. Open to participants aged 21 Years to 44 Years. Per ClinicalTrials.gov, last updated 2020-08-26.

Sponsored by University of North Carolina, Chapel Hill · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
21 Years to 44 Years
Sex
All
01

Study summary

The present proposal is an innovative and translational clinical trial derived from exciting preclinical findings to test the hypothesis that treatment with the melanocortin activator bupropion can reduce binge drinking in humans. Furthermore, pilot data on moderating effects of coexisting nicotine use on the efficacy of bupropion for binge drinking population will be obtained. Evidence for an efficacy signal with good tolerability with this FDA approved medication would form the foundation to conduct a well-powered Phase II b trial. The development of an effective pharmacotherapy for binge drinking would be a significant clinical advance.

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Read the detailed description

The design is a 1:1 random assignment to placebo or bupropion XL (extended release) (300mg/d). The study biostatistician, will prepare the randomization schedule and include blocking by gender and nicotine dependence. Randomization will be based on a stratified block design, with gender and nicotine dependence as the stratification variables with medication/placebo randomly assigned in blocks of four.

Bupropion XL will be initiated at 150 mg/d on Days 1-4 and increased to 300 mg/d for Days 5-84. The University of North Carolina (UNC) Hospital's Investigational Drug Services (IDS) will prepare opaque capsules containing bupropion XL 150/300 mg and matching placebo. Capsules will be inserted into blister packs with each pack containing 1 week of medication. The IDS will receive the randomization schedule from our statistician and prepare the blister packs according to the blocked schedule with blocking for gender/nicotine dependence.

Recruitment, Telephone Screen, and Full Eligibility Screening: Subjects will initially be prescreened by phone and then at full screening read and sign the informed consent. A breathalyzer test will be administered (must be 0.00 gms/dl to give informed consent), height, weight and BMI recorded and a medical history and examination completed. Over-the-counter and prescription medication use will be recorded and nicotine use documented. Complete Blood Count (CBC) with differential; serum bilirubin, Aspartate Aminotransferase (AST), Alanine Aminotransferase (ALT), Gamma-Glutamyl Transferase (GGT,) sodium, potassium, chloride, blood urea nitrogen, creatinine, glucose; and urinalysis and urine toxicology completed. Women will be given a urine pregnancy test (Ub-HCG) at screening and at weeks 4, 8, and 12. Trained interviewers will conduct the psychiatric screening interview using the M.I.N.I. . The Structured Clinical Interview (SCID) Substance Use Disorders Module to establish Diagnostic and Statistical Manual (DSM-V) criteria for alcohol use disorders will be administered by one of the study doctors. The study coordinator will conduct the pretreatment 90-day Timeline Followback (TLFB) interview to identify amount of alcohol consumed and timeframe of consumption. A binge drinking episode requires a minimum of 5/4 (men/women) standard drinks consumed over about a two hour period, i.e. consuming a bottle of wine over five hours would not be coded as a binge drinking day. The Penn Alcohol Craving Scale (PACS) and the University of Rhode Island Change Assessment (URICA) will be completed and treatment goal-abstinence vs. reduction- recorded.

Initial Treatment Visit (within 21 days screening): Eligible individuals will not be required to abstain from drinking alcohol prior to randomization. The study coordinator will administer a breathalyzer test (BAC must be ≤0.04 gms/d) and complete assessments as outlined in Table 1, Protection of Human Subjects. A salivary cotinine sample will be taken A 1-week blister pack of bupropion-XL or placebo with written instructions will be dispensed from the Investigational Drug Services according to the randomization block along with a 1-week back-up blister pack in case of delayed appointments or lost doses. Bupropion-XL will be titrated with 150 mg given daily for 4 days followed by 300 mg/d. Participants will be given a calendar style diary to track pill taking, drinking quantity/timing, intoxication and any side effects. Finally, participants will receive Medical Management from a trained clinician.

Subsequent Treatment Visits: TLFB and PACS are gathered each visit, cotinine samples at weeks 4, 8 and 12 and URICA at week 8. Medical monitoring will be conducted by study physicians and will consist of review of vital signs, concomitant medication use, and general inquiries into side effects. The physician may recommend that medication be held for a period of time to deal with an adverse event, e.g. nausea. One month and three months following the last visit subjects will be contacted by phone to update drinking (TLFB), adverse effects and medications.

Medical Management Intervention: The psychosocial support for the study will be Medical Management (MM). MM sessions average 10-15 minutes and focus on three main areas: (1) feedback on consequences of drinking; (2) encouraging compliance with medication/addressing compliance problems and (3) encouraging progress towards drinking goal- reduction or abstinence are acceptable. 10% of sessions will be audiotaped and reviewed to enhance fidelity.

Medication Compliance Monitoring: Participants will record their pill taking in calendar-style diaries that will be provided and collected at each visit. Pills will be distributed in blister packs that will be returned to the study coordinator to reconcile any unused medication from the returned blister packs with participants' diary records.

02

Conditions studied

  • Alcohol Abuse
03

Who can participate

Ages eligible
21 Years to 44 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Men and women between the ages of 21 and 44 years.
  2. A minimum of 5/3 (men/women) or more binge drinking episodes per month over the past three months. A binge drinking episode is defined as the consumption of 5/4 (men/women) standard drinks (\~12 gms ethanol) in about a two hour period. Subjects may meet DSM-V criteria for mild or moderate alcohol use disorder.
  3. Ability to understand and sign written informed consent.
  4. Must have a 0.0 gms/dl breathalyzer reading on the day of screening and 0.0 gms/dl on the day of randomization.
  5. BMI ≥18.5 (normal weight or above)
  6. Express a desire to achieve abstinence or to reduce alcohol consumption
  7. Must have a stable residence and be able to identify an individual who could contact participant if needed.

Exclusion criteria

Exclusion Criteria:

  1. Presence of physical dependence on alcohol as assessed by clear tolerance to alcohol or alcohol withdrawal symptoms based on SCID interview or a Severe Alcohol Use Disorder (>5 SCID DSM-V symptoms).
  2. Bupropion is contraindicated in individuals with a history of bulimia or a seizure disorder
  3. Clinically significant medical disease that might interfere with the evaluation of the study medication or present a safety concern (e.g., renal insufficiency, cirrhosis, unstable hypertension, diabetes mellitus, seizure disorder). Clinically significant psychiatric illness including any psychotic disorder, bipolar disorder, anorexia/bulimia, severe depression, or suicidal ideation.
  4. Other substance abuse or dependence disorder other than nicotine or cannabis abuse.
  5. Concurrent use of anticonvulsants. Concurrent use of any psychotropic medication including antidepressants, mood stabilizers, antipsychotics, anxiolytics, stimulants, or hypnotics with the exception of stable doses of antidepressants for one month. Bupropion is commonly added to antidepressants for augmentation so the use of another antidepressant does not represent a safety concern. .Prior history of adverse reaction to bupropion.
  6. AST or ALT > 3.5 times Upper Limit of Normal (ULN) or bilirubin > 1.5 X ULN.
  7. Positive urine toxicology screen with the exception of cannabis. Individuals with positive cannabis screens will be excluded only if they have a history of cannabis dependence.
  8. Pregnant women and women of childbearing potential who do not practice a medically acceptable form of birth control (oral or depot contraceptive, or barrier methods such as diaphragm or condom with spermicidal).
  9. Women who are breastfeeding.
  10. Individuals requiring inpatient treatment or more intense outpatient treatment for their alcohol problems.
  11. Participation in any clinical trial within the past 60 days that would have safety concerns for the trial.
  12. Court-mandated participation in alcohol treatment or pending incarceration.
04

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
42 participants (actual)

Study arms

  • Active comparator
    Bupropion

    Bupropion extended release

    Drug: Bupropion

  • Placebo comparator
    Placebo

    Placebo oral tablet

    Drug: Placebo Oral Tablet

Interventions

  • DrugBupropion

    Bupropion XL will be initiated at 150 mg/d on Days 1-4 and increased to 300 mg/d for Days 5-84.

    Also known as: Wellbutrin Extended Release

  • DrugPlacebo Oral Tablet

    Placebo will be initiated on Day 1 and continue throughout the course of the study.

    Also known as: Sugar pill

05

What researchers measure

Primary outcomes

  1. Change in Proportion of Binge Drinking Days

    Frequency is assessed as number of binge episodes/time in trial controlling for missing data.

    Time frame: Randomization (Week 0) to Week 12

  2. Change in the Intensity of Binge Drinking

    Intensity is defined as the number of drinks per binge day scaled by the minimum threshold of a binge episode per gender (4 drinks/day for females; 5 drinks/day for males). Accordingly, if a female consumed 4 drinks in a binge drinking day, the intensity would be 1.0 and a female who consumed 6 drinks in a binge drinking day would have an intensity of 1.5.

    Time frame: Randomization (Week 0) to Week 12

Secondary outcomes

  1. Change in GGT

    Change in serum Gamma-glutamyltransferase (GGT) levels

    Time frame: Randomization (Week 0) to Week 12

06

Results

Posted Aug 26, 2020

Participant flow

Participant flow — Overall Study
MilestoneBupropion XLPlacebo
Started2220
Randomly assigned2220
Received intervention2218
Completed1716
Not completed54
Withdrew: Lost to follow-up12
Withdrew: Adverse event10
Withdrew: Withdrawal by subject22
Withdrew: Physician decision10

Outcome measures

PrimaryChange in Proportion of Binge Drinking Days

Frequency is assessed as number of binge episodes/time in trial controlling for missing data.

Time frame:
Randomization (Week 0) to Week 12
Reported as:
Mean · Binge Drinking Days
Change in Proportion of Binge Drinking Days
Binge Drinking DaysBupropion XLPlacebo
Change in Proportion of Binge Drinking Days-0.13 ± 0.12-0.11 ± 0.09
PrimaryChange in the Intensity of Binge Drinking

Intensity is defined as the number of drinks per binge day scaled by the minimum threshold of a binge episode per gender (4 drinks/day for females; 5 drinks/day for males). Accordingly, if a female consumed 4 drinks in a binge drinking day, the intensity would be 1.0 and a female who consumed 6 drinks in a binge drinking day would have an intensity of 1.5.

Time frame:
Randomization (Week 0) to Week 12
Reported as:
Mean · unitless
Change in the Intensity of Binge Drinking
unitlessBupropion XLPlacebo
Change in the Intensity of Binge Drinking-0.02 ± 0.48-0.09 ± 0.41
SecondaryChange in GGT

Change in serum Gamma-glutamyltransferase (GGT) levels

Time frame:
Randomization (Week 0) to Week 12
Reported as:
Mean · U/L
Change in GGT
U/LBupropion XLPlacebo
Change in GGT12.8 ± 67.3-1.8 ± 9.75

Adverse events

Collected over From randomization through study follow-up, a total of approximately 16 weeks. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Bupropion XL0/22 (0%)0/22 (0%)11/22 (50%)
Placebo0/18 (0%)0/18 (0%)13/18 (72.2%)
Most frequent other events
Showing 10 of 12
Most frequent other events
EventBupropion XLPlacebo
HeadacheNervous system disorders3/228/18
NauseaGastrointestinal disorders4/224/18
InsomniaGeneral disorders4/221/18
Decreased AppetiteGastrointestinal disorders3/222/18
Dry MouthGeneral disorders3/221/18
RashSkin and subcutaneous tissue disorders2/220/18
AnxietyPsychiatric disorders1/221/18
Chest PainGeneral disorders0/221/18
PruritisSkin and subcutaneous tissue disorders1/220/18
SweatingGeneral disorders1/220/18

Baseline characteristics

Age, Continuous
Age, Continuous(years)Bupropion XLPlaceboTotal
Mean26.2 ± 7.2624.4 ± 3.5725.4 ± 5.89
Sex: Female, Male
Sex: Female, Male(Participants)Bupropion XLPlaceboTotal
Female151328
Male7512
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Bupropion XLPlaceboTotal
Hispanic or Latino336
Not Hispanic or Latino191534
Unknown or Not Reported000
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Bupropion XLPlaceboTotal
American Indian or Alaska Native000
Asian314
Native Hawaiian or Other Pacific Islander000
Black or African American516
White141327
More than one race000
Unknown or Not Reported033
Region of Enrollment
Region of Enrollment(Participants)Bupropion XLPlaceboTotal
United States221840
Marital Status
Marital Status(Participants)Bupropion XLPlaceboTotal
Married336
Divorced/Separated101
Single, Never Married181533
Years Education
Years Education(years)Bupropion XLPlaceboTotal
Mean15.7 ± 2.2716.2 ± 1.4816.0 ± 1.95
Smoking History
Smoking History(Participants)Bupropion XLPlaceboTotal
Never Smoked171532
Less than or equal to 1/2 Pack/Day235
Greater than or equal to 1 Pack/Day101

5 further baseline measures are reported on the registry.

07

Study locations

1 site
  • University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina 27599, United States
08

References and documents

Study documents

  • Protocol and statistical analysis plan · Aug 26, 2019

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Registry details

Key details

Study ID
NCT03169244
Lead sponsor
University of North Carolina, Chapel Hill
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Responsible party
James Garbutt, MD (Professor of Medicine, University of North Carolina, Chapel Hill) — Principal investigator
First posted
May 30, 2017
Start date
Sep 4, 2017
Primary completion
Aug 19, 2019
Completion
Sep 17, 2019
Results posted
Aug 26, 2020
Last update
Aug 26, 2020

Study contacts

James C Garbutt
principal investigator · UNC Chapel Hill

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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