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NCT00004552 · ClinicalTrials.gov registry record · Phase 2

Acamprosate Treatment: Mechanisms of Action

A Phase 2 study, sponsored by Yale University.

Completed
Registry status
Phase 2
Development phase
120
Enrollment target

NCT00004552 is a Phase 2 study that has completed, run by Yale University. The registered enrollment target is 120 participants.

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The verdict

NCT00004552, a Phase 2 study, has completed, sponsored by Yale University.

COMPLETED
Registry status
Phase 2
Development phase
120 participants
Enrollment target

Study Summary

This study will examine whether pretreatment with two doses of acamprosate for seven days prior to abstinence lessens the intensity of acute withdrawal from alcohol compared with a placebo. Subjects will be randomly assigned to receive either one of two doses of acamprosate or placebo for seven days. This will be followed by a four- day inpatient period when withdrawal will be monitored. Additional drinking information will be obtained at a three month followup interview.

Interventions

  • DRUG acamprosate (Campral)

Trial Details

FieldValue
Enrollment Target 120 participants
Est. Completion 2002-12
Phase Phase 2

Sponsor

Yale University

1,492 total trials

What the Registry Record Tells You About NCT00004552

The ClinicalTrials.gov registry entry for NCT00004552 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Yale University, which has 1,492 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which acamprosate (Campral) is the first listed.

NCT00004552 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00004552 about?

NCT00004552 is a clinical study titled "Acamprosate Treatment: Mechanisms of Action". This study will examine whether pretreatment with two doses of acamprosate for seven days prior to abstinence lessens the intensity of acute withdrawal from alcohol compared with a placebo. Subjects will be randomly assigned to receive either one of two doses of acamprosate or placebo for seven days...

What is the current status of trial NCT00004552?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 120 participants. Estimated completion is 2002-12.

What interventions are being tested in trial NCT00004552?

The interventions under investigation include: acamprosate (Campral) (DRUG).

Who is sponsoring clinical trial NCT00004552?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.