CClinicalTrials.gg
CompletedNCT01573052Updated Aug 17, 2020Results posted

Gabapentin vs Chlordiazepoxide for Ambulatory Alcohol Withdrawal

A Phase 4 interventional study of Chlordiazepoxide and Gabapentin in Alcohol Withdrawal, sponsored by VA Salt Lake City Health Care System. Completed at 1 site in United States. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2020-08-17.

Sponsored by VA Salt Lake City Health Care System · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
26
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
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Study summary

A randomized, double-blind controlled trial comparing treatment outcomes between chlordiazepoxide, or gabapentin to treat alcohol withdrawal syndrome in alcohol dependent veteran subjects. The objective of this trial is to compare the safety and effectiveness of these two medications. Intervention is a fixed dose taper of chlordiazepoxide, or gabapentin over 6 days. Subjects will be evaluated for 7-10 days to monitor alcohol abstinence, withdrawal severity scores, adverse events including ataxia, sedation, cognitive function and alcohol craving.

Read the detailed description

Chlordiazepoxide 25 mg and matching placebo capsules or gabapentin 300 mg and matching placebo capsules were were used. The chlordiazepoxide/placebo and gabapentin/placebo capsules were not identical in appearance. Study medications were packaged into a 7-day medication organizer. The dosing for each subject was either gabapentin 1200mg or chlordiazepoxide 100 mg orally days 1-3, gabapentin 900 mg or chlordiazepoxide 75 mg day 4, gabapentin 600 mg or chlordiazepoxide 50 mg day 5, and gabapentin 300 mg or chlordiazepoxide 25 mg day 6.

Adherence was assessed by pill counts and serum samples were obtained for study drug analysis. Serum samples were batched and sent to a contract laboratory so that study clinicians were blinded to the results until after the trial was completed. Presence of the assigned study medication in the blood served as a surrogate adherence marker.

Subjects also received prescriptions for daily oral therapeutic multiple vitamin tablets, folic acid 1 mg, and thiamine 100 mg.

A psychiatric history and physical examination, breath alcohol concentration, vital signs, CIWA-Ar (alcohol withdrawal scale), and blood chemistry including transaminases and complete blood cell count were obtained for baseline for all participants. Subjects were seen on weekdays for clinic follow-up appointments. Assessments performed at each study visit included CIWA-Ar, ESS (Epworth Sleepiness Scale), PACS (Penn Alcohol Craving Scale), and a brief examination to document mental status and assess coordination, which included assessment of stance, tandem gait, Romberg test, pronator drift, toe and heel walk, rapid-alternating-movements, and point-to-point movements. Breath alcohol concentration (BAC) was also measured (AlcoSensor, Intoximeters, Inc.) at each visit.

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Conditions studied

  • Alcohol Withdrawal
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In context

Lead sponsor

VA Salt Lake City Health Care System is the lead sponsor of 10 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Alcohol dependent at risk for withdrawal symptoms

Exclusion criteria

Exclusion Criteria:

  • Benzodiazepine dependent
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Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
26 participants (actual)

Study arms

  • Active comparator
    Chlordiazepoxide

    Chlordiazepoxide 25mg capsule or matching placebo capsule

    Drug: Chlordiazepoxide

  • Experimental
    Gabapentin

    Gabapentin 300mg capsule or matching placebo capsule

    Drug: Gabapentin

Interventions

  • DrugChlordiazepoxide

    25mg four times daily x 3 days then tapered over 3 days

    Also known as: Librium

  • DrugGabapentin

    300mg four times daily x 3 days then tapered over 3 days

    Also known as: Neurontin

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What researchers measure

Primary outcomes

  1. Epworth Sleepiness Scale (ESS)

    ESS is an 8 item-scale and scores range between 0 and 24. The higher the score implies more daytime sleepiness.

    Time frame: 1 week

  2. PENN Alcohol Craving Scale

    PENN is a 5 item self-rated scale of alcohol craving. Scores range from 0 (little craving for alcohol) to 30 (irresistable urge to drink alcohol)

    Time frame: 1 week

Secondary outcomes

  1. Clinical Institute Withdrawal Assessment-Alcohol (Revised)(CIWA-Ar)

    CIWA-Ar measures severity of 10 observed or measured alcohol withdrawal signs or symptoms. Total score ranges from 0 (best possible outcome)-67 (worst possible outcome). Many previously publications suggest a total score of 8-10 is severe enough to warrant medication treatment. Lower scores (0-8) represent fewer withdrawal symptoms and less severity, scores \> 8 represent more withdrawal symptoms and greater severity

    Time frame: 1 week

07

Results

Posted Aug 17, 2020

Participant flow

Subjects recruited from VA outpatient detoxification clinic

Participant flow — Overall Study
MilestoneChlordiazepoxideGabapentin
Started917
Completed611
Not completed36

Outcome measures

PrimaryEpworth Sleepiness Scale (ESS)

ESS is an 8 item-scale and scores range between 0 and 24. The higher the score implies more daytime sleepiness.

Time frame:
1 week
Reported as:
Mean · units on a scale
Epworth Sleepiness Scale (ESS)
units on a scaleChlordiazepoxideGabapentin
Epworth Sleepiness Scale (ESS)6.35 (3.13 to 9.57)2.65 (0.44 to 4.85)
PrimaryPENN Alcohol Craving Scale

PENN is a 5 item self-rated scale of alcohol craving. Scores range from 0 (little craving for alcohol) to 30 (irresistable urge to drink alcohol)

Time frame:
1 week
Reported as:
Mean · units on a scale
PENN Alcohol Craving Scale
units on a scaleChlordiazepoxideGabapentin
PENN Alcohol Craving Scale16.78 (10.92 to 22.64)10.74 (7.09 to 14.39)
SecondaryClinical Institute Withdrawal Assessment-Alcohol (Revised)(CIWA-Ar)

CIWA-Ar measures severity of 10 observed or measured alcohol withdrawal signs or symptoms. Total score ranges from 0 (best possible outcome)-67 (worst possible outcome). Many previously publications suggest a total score of 8-10 is severe enough to warrant medication treatment. Lower scores (0-8) represent fewer withdrawal symptoms and less severity, scores \> 8 represent more withdrawal symptoms and greater severity

Time frame:
1 week
Reported as:
Mean · units on a scale
Clinical Institute Withdrawal Assessment-Alcohol (Revised)(CIWA-Ar)
units on a scaleChlordiazepoxideGabapentin
Clinical Institute Withdrawal Assessment-Alcohol (Revised)(CIWA-Ar)3.29 (-0.28 to 6.88)4.33 (2.10 to 6.56)

Adverse events

Collected over 7 days. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Chlordiazepoxide—0/9 (0%)0/9 (0%)
Gabapentin—0/17 (0%)0/17 (0%)

Baseline characteristics

Age, Continuous
Age, Continuous(years)ChlordiazepoxideGabapentinTotal
Mean55.8 ± 4.851.1 ± 7.752.7 ± 6.6
Sex: Female, Male
Sex: Female, Male(Participants)ChlordiazepoxideGabapentinTotal
Female101
Male81725
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Study locations

1 site
  • George E Wahlen VA Medical Center
    Salt Lake City, Utah 84148, United States
09

References and documents

Publications

  • Stock CJ, Carpenter L, Ying J, Greene T. Gabapentin versus chlordiazepoxide for outpatient alcohol detoxification treatment. Ann Pharmacother. 2013 Jul-Aug;47(7-8):961-9. doi: 10.1345/aph.1R751. Epub 2013 Jun 18. PubMed 23780805 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 17, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01573052
Lead sponsor
VA Salt Lake City Health Care System
Responsible party
Christopher J. Stock, PharmD (Investigational pharmacist, VA Salt Lake City Health Care System) — Principal investigator
First posted
Apr 6, 2012
Start date
Mar 2004
Primary completion
Aug 2010
Completion
Sep 2010
Results posted
Aug 17, 2020
Last update
Aug 17, 2020

Study contacts

Christopher J Stock, PharmD
principal investigator · Salt Lake VA Health Care System

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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