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Comparing Gabapentin and Lorazepam for Treating Alcohol Withdrawal

Alcohol Research Center - Treatment and Implications

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00011297
Enrollment
160
Registered
2001-02-19
Start date
Unknown
Completion date
2005-12-31
Last updated
2006-10-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcoholism

Brief summary

This study will evaluate a safe and useful medication for outpatient detoxification that is as effective as benzodiazepines in the short-term, and more effective in the protracted withdrawal period. Gabapentin (Neurontin) will be compared to a standard benzodiazepine, lorazepam (Ativan), for its effectiveness in treating alcohol withdrawal.

Interventions

Sponsors

National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Meets criteria for alcohol dependence and uncomplicated alcohol withdrawal syndrome. * Subjects must be medically stable (not likely to require hospitalization for medical complications within 10 days). * Have a clinical withdrawal assessment prior to study. * 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. * Able to read, write, and speak English. * Have a negative urine drug screen for benzodiazepines or other sedative hypnotics, opiates, and stimulates prior to entering the study.

Exclusion criteria

* Current diagnosis of any other substance dependence syndrome other than alcohol dependence (excluding nicotine and caffeine dependence). * Use of pharmacological agents within the last 14 days that are known to lower the seizure threshold or augment or decrease the alcohol withdrawal syndrome. * History of alcohol withdrawal seizures, epilepsy or delirium tremens. * Diagnosis of schizophrenia, bipolar disorder or dementia. * Liver function tests higher than normal. * History of hepatic encephalopathy, jaundice, ascites, diabetes, or renal disease. * Females who are pregnant or nursing. * Subjects with known sensitivity of 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. * Unable to provide an informed consent.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026