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Acamprosate Initiated During Alcohol Detoxification

10. Januar 2017 aktualisiert von: Forest Laboratories

Initiating Acamprosate Within Versus Post-detoxification in the Rehabilitative Treatment of Alcohol Dependence.

Acamprosate is approved by the Food and Drug Administration (FDA) for the treatment of alcoholism. The purpose of this study is to see if initiating acamprosate early in alcohol detoxification instead of waiting until detoxification has been completed effects the course of detoxification, adverse events during detoxification, drop out rate during the rehabilitative treatment phase, or overall efficacy of acamprosate for those with alcohol dependence who plan to receive at least two months of rehabilitative pharmacotherapy with acamprosate.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Detaillierte Beschreibung

Biphasic clinical trial, consisting of a randomized, double-blind, placebo-controlled detoxification treatment phase (DP), followed by 9-week open-label rehabilitative treatment phase (RP).

Studientyp

Interventionell

Einschreibung (Tatsächlich)

40

Phase

  • Phase 2

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Pennsylvania
      • Philadelphia, Pennsylvania, Vereinigte Staaten, 19104
        • Treatment Research Center

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 70 Jahre (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria for Detoxification Treatment Phase

  1. Males and females from the ages of 18 to 70 years old. Subjects over the age of 70 years old will be included at the discretion of the PI, with the expectation that these subjects should comprise of no more than 5% of the subjects.
  2. Diagnosis of current alcohol dependence according to DSM-IV criteria [DSM-IV criteria will be determined by utilizing the Mini International Neuropsychiatric Interview (MINI)].
  3. If necessary, can be medically detoxified in the outpatient setting, as determined by a medical clinician.
  4. Meets the following drinking criteria, measured by TLFB: a. reports a minimum of 48 standard alcoholic drinks (avg 12 drinks/wk) in a consecutive 30-day period over the 90-day period prior to starting pharmacotherapy, b. has 2 or more days of heavy drinking (defined as 5 or more drinks per day in males and 4 or more drinks per day in females) within 30 days of starting pharmacotherapy treatment and c. has had a drink within 48 hours of the intake/screening visit or has a CIWA score equal to or greater than 3.
  5. Speaks, understands and prints in English.
  6. Gives written informed consent.

Exclusion Criteria for Detoxification Treatment Phase (DP)

  1. Subjects mandated to treatment based upon a legal decision or as a condition of employment.
  2. Subjects with evidence of substance dependence other than alcohol or nicotine dependence.
  3. Subjects with psychosis or dementia at the time of the initial evaluation.
  4. Female Subjects who are pregnant or lactating, or female Subjects of child bearing potential who are not using acceptable methods of birth control. Acceptable methods of birth control include: tubal ligation, barrier (diaphragm or condom) with spermicide, intrauterine progesterone contraceptive system, levonorgestrel implant, medroxyprogesterone acetate contraceptive injection, and oral contraceptives.
  5. Clinical laboratory tests (CBC, blood chemistries, urinalysis) outside normal limits that are clinically unacceptable to the Principal Investigator. EKG first degree heart block, sinus tachycardia, left axis deviation, and nonspecific ST or T wave changes are allowed; liver function tests [LFTs] <5 x ULN are acceptable), Subjects with impaired renal function as indicated by corrected creatinine clearance below 80 ml/min/70 kg as determined by the modified Cockcroft equation (CDC, 1986).
  6. Subjects who have a positive urine drug screening (cocaine, amphetamines, opiates, barbiturates, benzodiazepines)
  7. Subjects who have any disease of the gastrointestinal tract, liver or kidneys that could result in a possibility of altered metabolism or excretion of the study drug. As it is not possible to enumerate the many conditions which might impair absorption, metabolism, or excretion, the investigators will be guided by evidence such as: History of major gastrointestinal tract surgery (gastrectomy, gastrostomy, bowel resection, etc.) or a history of an active peptic ulcer or chronic disease of the GI tract, (ulcerative colitis, regional enteritis, or gastrointestinal bleeding).
  8. Current unstable heart disease.
  9. Known hypersensitivity to acamprosate.
  10. Subjects taking psychotropic drugs (e.g., antidepressants, anxiolytic, antipsychotic, naltrexone, disulfiram, modafinil, stimulants and anticonvulsants) with the exception of oxazepam
  11. Subjects receiving formal psychotherapy
  12. Subjects having participated in any investigational drug trial within 30 days prior to the study.
  13. Subjects with AIDS or other serious illnesses that may require hospitalization during the study.

Inclusion Criteria for Post-Detoxification Rehabilitative Treatment Phase (RP/Phase 2) with Open-Label Acamprosate

  1. Has taken at least 5 days of acamprosate or placebo directly prior to initiating open-label acamprosate.
  2. Successfully completed, within a 14-day period, outpatient detoxification. Successful completion of detoxification is defined as having a score of 1 or lower on the Clinical Institutes Withdrawal Assessment for Alcohol (CIWA; Shaw et al., 1981), and has at least 3 consecutive days of abstinence.
  3. Has reduced medication taken specifically for detoxification (if applicable), i.e., oxazepam to 45 mg within 24-hour period prior to the post-detoxification rehabilitative treatment phase.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Vervierfachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Placebo-Komparator: 2
Placebo
3 pills (666mg) for 1998mg/day
Experimental: 1
Acamprosate
3 pills (666 mg) for 1998mg/day
Andere Namen:
  • Campral

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
1) the mean number of adverse events rated moderate to severe;
Zeitfenster: Phase I: up to 2 weeks
Phase I: up to 2 weeks
2) the week of detoxification treatment discontinuation;
Zeitfenster: Phase I: up to 2 weeks
Phase I: up to 2 weeks
3) the total amount of oxazepam given;
Zeitfenster: Phase I: up to 2 weeks
Phase I: up to 2 weeks
4) the rate of change in CIWA scores.
Zeitfenster: Phase I: up to 2 weeks
Phase I: up to 2 weeks
1) the mean number of adverse events rated moderate to severe;
Zeitfenster: Phase II: 10 weeks
Phase II: 10 weeks
2) the week of open-label treatment discontinuation;
Zeitfenster: Phase II: 10 weeks
Phase II: 10 weeks
3) any reemergence of detoxification symptoms;
Zeitfenster: Phase II: 10 weeks
Phase II: 10 weeks
4) % pills taken over what was proposed to be prescribed (medication exposure);
Zeitfenster: Phase II: 10 weeks
Phase II: 10 weeks
5) % days abstinent;
Zeitfenster: Phase II: 10 weeks
Phase II: 10 weeks
6) % days heavy drinking.
Zeitfenster: Phase II: 10 weeks
Phase II: 10 weeks

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Changes in alcohol craving will be measured by Penn Alcohol Craving Scale (PACS; Flannery et al, 1999)
Zeitfenster: 12 weeks
12 weeks
Changes in anxiety symptoms will be measured by the Structured Interview Guide for the Hamilton Anxiety Rating Scale (SIGH-A; Hamilton, 1969)
Zeitfenster: 12 weeks
12 weeks
Changes in depressive symptoms will be measured by the Structured Interview Guide for the Hamilton Depression Rating Scale (SIGH-D; Hamilton 1967)
Zeitfenster: 12 weeks
12 weeks
Changes in social functioning will be measured by several of the subscales of the Addiction Severity Index (ASI; McLellan et al, 1992); namely, medical, legal, psychiatric, and family/social.
Zeitfenster: 12 weeks
12 weeks
Quality of Life, measured by the Short Form-36 Health Status Questionnaire (SF-36; Ware & Sherbourne, 1999)
Zeitfenster: 12 weeks
12 weeks
Overall clinical impression of improvement will be measured by the Clinical Global Impression Scale (CGI)
Zeitfenster: 12 weeks
12 weeks

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Helen Pettinati, Ph.D., UNIVERSITY of PENNSYLVANIA

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. Oktober 2006

Primärer Abschluss (Tatsächlich)

1. September 2007

Studienabschluss (Tatsächlich)

1. November 2007

Studienanmeldedaten

Zuerst eingereicht

2. August 2006

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

2. August 2006

Zuerst gepostet (Schätzen)

4. August 2006

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

11. Januar 2017

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

10. Januar 2017

Zuletzt verifiziert

1. Juni 2010

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Andere Studien-ID-Nummern

  • 804481
  • DPMC (Andere Kennung: NIDA)
  • P50DA012756-07 (US NIH Stipendium/Vertrag)
  • CMP-MD-08

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