Status:

COMPLETED

Effects of Ghrelin on Alcohol Cue Reactivity and Craving

Lead Sponsor:

Brown University

Conditions:

Alcoholism

Eligibility:

All Genders

18-70 years

Phase:

NA

Brief Summary

Only a few medications are approved for the treatment of alcohol dependence and there exists a substantial need for discovering ways to provide more effective treatments. Accordingly, identifying new ...

Eligibility Criteria

Inclusion

  • Understanding that this is not a treatment study.
  • Breath alcohol concentration (BAC) equal to 0.00 when the participants sign the informed consent document.
  • Age between 18 and 70 years old (inclusive).
  • Female participants must be postmenopausal for at least one year, surgically sterile, or practicing an effective method of birth control before entry and throughout the study; have a negative urine pregnancy test at screening and cue-reactivity (CR) visits.
  • Diagnosis of Alcohol dependence using Module E of the structured clinical interview for the Diagnostic and Statistical Manual of Mental Disorders - Text Revised (DSM-IV-TR).
  • Participants must meet criteria for heavy drinking, defined as averaging ≥4 drinks/day for women and ≥5 drinks/day for men during a consecutive 30-day period within the 90 days prior to baseline evaluation
  • Good health as confirmed by medical history, physical examination, electrocardiogram (ECG), laboratory tests and vital signs.
  • Participant must be willing to receive an I.V. line.

Exclusion

  • Individuals expressing interest in treatment for alcoholism.
  • Females who are of child bearing potential and not practicing effective birth control.
  • Current (last 12 months) diagnosis of dependence on any psychoactive substance other than alcohol and nicotine (according to the DSM-IV-TR)
  • DSM-IV-TR Axis I criteria for a lifetime diagnosis of schizophrenia, bipolar disorder, or other psychoses; an active illness within the past 6 months that meet the DSM-IV-TR criteria for a diagnosis of Major Depressive Disorder or Anxiety Disorder; in the investigators' opinion, moderate to severe risk of suicide (e.g. active plan, or attempt in last 6 months).
  • History of hospitalization for alcohol intoxication delirium, alcohol withdrawal delirium or seizure.
  • Clinical Institute Withdrawal Assessment for Alcohol revised (CIWA-Ar) ≥ 10, at any assessment.
  • Positive urine drug screen at baseline for any illegal substance other than marijuana (a urine drug screen may be repeated once during the screening period).
  • Subjects who have received any behavioral and/or pharmacological treatment for alcoholism within the past 30 days.
  • Current use of psychotropic medications that cannot be discontinued.
  • Clinically significant medical abnormalities \[e.g., alanine aminotransferase (ALT) or aspartate aminotransferase (AST) \>300% the upper limit of normal\].
  • Significant medical conditions, such as cancer, liver cirrhosis, heart chronic failure, chronic kidney failure, chronic intestinal diseases (e.g., Crohn's disease), chronic neurological disorders (e.g., tardive dyskinesia, epilepsy, Parkinson's disease), diabetes, obesity \[Body Mass Index(BMI) ≥ 30 kg/m2\].
  • Participants with a history of hypotension clinically significant (e.g.: history of fainting and/or syncopal attacks).
  • No history of adverse reactions or hypersensitivity to ghrelin i.v. nor history of adverse reactions to needle puncture.

Key Trial Info

Start Date :

April 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

Estimated Enrollment :

45 Patients enrolled

Trial Details

Trial ID

NCT01190085

Start Date

April 1 2011

Last Update

May 15 2014

Active Locations (1)

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Brown University Center for Alcohol and Addiction Studies

Providence, Rhode Island, United States, 02903