Overview

Comparing the Treatment of Alcohol Withdrawal Syndrome Using Gabapentin Versus Lorazepam

Status:
Completed
Trial end date:
2005-09-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study was to evaluate if the medication Gabapentin, which is not approved for the treatment of alcohol withdrawal, is effective in the treatment of alcohol withdrawal syndrome compared to treatment with Lorazepam.
Phase:
Phase 2
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Treatments:
Ethanol
Gabapentin
gamma-Aminobutyric Acid
Lorazepam
Criteria
Inclusion Criteria:

- Subjects must be between 21-70 years of age (both genders will be recruited).

- Subjects must meet DSM-IV criteria for alcohol dependence and uncomplicated alcohol
withdrawal syndrome.

- Subjects must have a mini-mental state score above 26.

- Subjects must be medically stable (not likely to require hospitalization for medical
complications within 10 days).

- Subjects must have a minimum score on the Clinical Institute Withdrawal - - Assessment
for Alcohol-Revised (CIWA-Ar) of 10 within 24 hours of initial assessment.

- Subjects must be medically acceptable for study treatment. Considerations include no
past or present physical disorder that is likely to deteriorate during participation.
No ECG abnormality which would likely worsen during participation and no clinical
laboratory abnormality that would also suggest deterioration during treatment.

- Subjects must exhibit vital signs within the following range: a three-minute sitting
blood pressure in the range of 90-200 mmHg systolic, 60-120 mmHg diastolic and
ventricular rates between 56 and 140 beats per minute.

- Subjects must be suitable for treatment with oral medications.

- Subjects must be able to read, write, and speak English.

- Subjects must have a negative urine drug screen for benzodiazepines or other
sedative-hypnotics, opiates, and stimulants at baseline.

Exclusion Criteria:

- Subjects with current (past month) DSM-IV diagnosis of any other substance dependence
syndrome other than alcohol dependence (excluding nicotine, caffeine, cannabis and
cocaine dependence).

- Use of pharmacological agents within a five half-life period that are known to lower
the seizure threshold or augment or decrease the alcohol withdrawal syndrome
(e.g.,tricyclic antidepressants, anticonvulsants, neuroleptics, benzodiazepines, some
centrally-acting antihypertensives such as beta-blockers, alpha-adrenergic agonists,
and calcium channel antagonists, wellbutrin, buspar, any sedative-hypnotics and
opiates).

- Subjects with a history of idiopathic epilepsy.

- Subjects with diagnosis of schizophrenia, bipolar disorder or dementia.

- Subjects with liver function tests (AST or ALT) 4 times higher than normal. Serum
levels will be drawn upon admission to study and study medications terminated if
necessary.

- History of hepatic encephalopathy, jaundice, ascites, insulin dependent diabetes, or
renal disease.

- Females who are pregnant (as determined by a pregnancy test) or nursing.

- Subjects with known sensitivity or previous adverse reaction to gabapentin, lorazepam,
or other benzodiazepines.

- History of severe GI disease which might render absorption of the medication difficult
or produce medical instability of the patient during detoxification which would
include active peptic ulcer disease, ulcerative colitis, regional colitis, or evidence
by history or physical exam of GI bleeding.

- Subjects who decline or who are not competent to give informed consent.