- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT00360594
Acamprosate Initiated During Alcohol Detoxification
2017년 1월 10일 업데이트: 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.
연구 개요
상세 설명
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).
연구 유형
중재적
등록 (실제)
40
단계
- 2 단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
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Pennsylvania
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Philadelphia, Pennsylvania, 미국, 19104
- Treatment Research Center
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참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
18년 (성인, 고령자)
건강한 자원 봉사자를 받아들입니다
아니
연구 대상 성별
모두
설명
Inclusion Criteria for Detoxification Treatment Phase
- 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.
- Diagnosis of current alcohol dependence according to DSM-IV criteria [DSM-IV criteria will be determined by utilizing the Mini International Neuropsychiatric Interview (MINI)].
- If necessary, can be medically detoxified in the outpatient setting, as determined by a medical clinician.
- 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.
- Speaks, understands and prints in English.
- Gives written informed consent.
Exclusion Criteria for Detoxification Treatment Phase (DP)
- Subjects mandated to treatment based upon a legal decision or as a condition of employment.
- Subjects with evidence of substance dependence other than alcohol or nicotine dependence.
- Subjects with psychosis or dementia at the time of the initial evaluation.
- 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.
- 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).
- Subjects who have a positive urine drug screening (cocaine, amphetamines, opiates, barbiturates, benzodiazepines)
- 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).
- Current unstable heart disease.
- Known hypersensitivity to acamprosate.
- Subjects taking psychotropic drugs (e.g., antidepressants, anxiolytic, antipsychotic, naltrexone, disulfiram, modafinil, stimulants and anticonvulsants) with the exception of oxazepam
- Subjects receiving formal psychotherapy
- Subjects having participated in any investigational drug trial within 30 days prior to the study.
- 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
- Has taken at least 5 days of acamprosate or placebo directly prior to initiating open-label acamprosate.
- 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.
- 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.
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 네 배로
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
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위약 비교기: 2
위약
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3 pills (666mg) for 1998mg/day
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실험적: 1
Acamprosate
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3 pills (666 mg) for 1998mg/day
다른 이름들:
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
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1) the mean number of adverse events rated moderate to severe;
기간: Phase I: up to 2 weeks
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Phase I: up to 2 weeks
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2) the week of detoxification treatment discontinuation;
기간: Phase I: up to 2 weeks
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Phase I: up to 2 weeks
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3) the total amount of oxazepam given;
기간: Phase I: up to 2 weeks
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Phase I: up to 2 weeks
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4) the rate of change in CIWA scores.
기간: Phase I: up to 2 weeks
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Phase I: up to 2 weeks
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1) the mean number of adverse events rated moderate to severe;
기간: Phase II: 10 weeks
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Phase II: 10 weeks
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2) the week of open-label treatment discontinuation;
기간: Phase II: 10 weeks
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Phase II: 10 weeks
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3) any reemergence of detoxification symptoms;
기간: Phase II: 10 weeks
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Phase II: 10 weeks
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4) % pills taken over what was proposed to be prescribed (medication exposure);
기간: Phase II: 10 weeks
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Phase II: 10 weeks
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5) % days abstinent;
기간: Phase II: 10 weeks
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Phase II: 10 weeks
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6) % days heavy drinking.
기간: Phase II: 10 weeks
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Phase II: 10 weeks
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2차 결과 측정
결과 측정 |
기간 |
|---|---|
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Changes in alcohol craving will be measured by Penn Alcohol Craving Scale (PACS; Flannery et al, 1999)
기간: 12 weeks
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12 weeks
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Changes in anxiety symptoms will be measured by the Structured Interview Guide for the Hamilton Anxiety Rating Scale (SIGH-A; Hamilton, 1969)
기간: 12 weeks
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12 weeks
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Changes in depressive symptoms will be measured by the Structured Interview Guide for the Hamilton Depression Rating Scale (SIGH-D; Hamilton 1967)
기간: 12 weeks
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12 weeks
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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.
기간: 12 weeks
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12 weeks
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Quality of Life, measured by the Short Form-36 Health Status Questionnaire (SF-36; Ware & Sherbourne, 1999)
기간: 12 weeks
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12 weeks
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Overall clinical impression of improvement will be measured by the Clinical Global Impression Scale (CGI)
기간: 12 weeks
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12 weeks
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공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
수사관
- 수석 연구원: Helen Pettinati, Ph.D., University of Pennsylvania
간행물 및 유용한 링크
연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작
2006년 10월 1일
기본 완료 (실제)
2007년 9월 1일
연구 완료 (실제)
2007년 11월 1일
연구 등록 날짜
최초 제출
2006년 8월 2일
QC 기준을 충족하는 최초 제출
2006년 8월 2일
처음 게시됨 (추정)
2006년 8월 4일
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
2017년 1월 11일
QC 기준을 충족하는 마지막 업데이트 제출
2017년 1월 10일
마지막으로 확인됨
2010년 6월 1일
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .