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The Role of Bacterial Overgrowth and Delayed Intestinal Transit in Hepatic Encephalopathy

2010년 11월 4일 업데이트: Weill Medical College of Cornell University

The Role of Bacterial Overgrowth and Delayed Intestinal Transit in Hepatic Encephalopathy. Phase A: Breath Testing and Colonic Transit in Hepatic Encephalopathy. Phase B: A Randomized Double Blind, Placebo Controlled Trial of Rifaximin for Hepatic Encephalopathy

The study will be conducted in two phases. Phase A will evaluate the contribution of bacterial overgrowth and colonic inertia to development of Hepatic Encephalopathy (HE)in 50 ambulatory subjects with HE and hepatitis C cirrhosis. This phase will include a Screening and Evaluation Visit.

Phase B will evaluate the effect of rifaximin on bacterial outgrowth and severity of HE in 20 of the subjects enrolled in Phase A who have a somewhat greater degree of encephalopathy.

The purpose of this study is to evaluate the following:

  1. the relationship between bacterial overgrowth and the presence and severity of HE in patients with hepatitis C cirrhosis;
  2. the effectiveness and tolerability of rifaximin relative to placebo in treatment of HE associated with hepatitis C cirrhosis;
  3. the relationship between bacterial overgrowth and the presence and severity of HE before and after rifaximin treatment.

연구 개요

상태

알려지지 않은

상세 설명

Hepatic encephalopathy is a frequent and occasionally refractory complication of cirrhosis and is associated with impaired quality of life. Its severity may not correlate with other parameters of liver dysfunction. Although multiple pathogenic mechanisms for the condition have been proposed, most include the participation of bacterial toxins, especially ammonia, produced in the gastrointestinal tract. Treatment options for hepatic encephalopathy at this time are limited to lactulose and neomycin. Lactulose is frequently poorly tolerated, and many patients are non-compliant with its use. In patients with renal insufficiency in whom hepatic encephalopathy is frequently problematic, use of neomycin is contraindicated due to ototoxicity and nephrotoxicity.

Autonomic dysfunction is common in patients with cirrhosis and could contribute to the development of hepatic encephalopathy by impairment of intestinal motility, leading to bacterial overgrowth and colonic inertia.

The following questions will be addressed:

A. Is impaired intestinal transit and bacterial overgrowth associated with the presence and severity of hepatic encephalopathy?

50 patients will undergo a detailed clinical evaluation for severity of liver disease, hepatic encephalopathy and assessment of intestinal transit and bacterial overgrowth with radiographic marker study and breath test analysis. Multivariate analysis will then be performed to determine the relationship of intestinal transit and evidence of bacterial overgrowth with the presence and severity of hepatic encephalopathy.

B. Does treatment with rifaximin improve bacterial overgrowth and hepatic encephalopathy?

20 patients from the above population with significant encephalopathy will be randomized to receive either rifaximin or placebo. Post-treatment evaluation for severity of hepatic encephalopathy and breath test analysis for bacterial overgrowth will then be performed. The effect of treatment on changes in hepatic encephalopathy and bacterial overgrowth and the relationship between changes in bacterial overgrowth and severity of hepatic encephalopathy will also be assessed.

Phase A Endpoints: Degree of bacterial overgrowth and its correlation with the grade of hepatic encephalopathy (if present).

Phase B Endpoints: To demonstrate improvement in degree of HE with treatment of Rifaximin

Efficacy Endpoints The primary efficacy endpoint for Phase B of the study will be the change from baseline in the proportion of patients with no HE, minimal HE (no symptoms, abnormal psychometric testing), mild persistent HE (mild symptoms), and persistent Stage II HE (presence of asterixis, history of hospitalization for spontaneous Stage III or IV HE).

Secondary efficacy endpoints for Phase B will be the following:

To demonstrate improvement in intestinal transit time for patients (based on Lactulose Hydrogen Breath Test) To demonstrate improvement in bacterial overgrowth, improved insomnia, flatulence, and quality of life.

To demonstrate that rifaximin improved patients' symptoms of insomnia, flatulence, and quality of life measure with the degree of bacterial overload and the impaired intestinal transit time.

연구 유형

중재적

등록 (예상)

50

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • New York
      • New York, New York, 미국, 10021
        • 모병
        • New York Presbyterian Hospital: Weill Medical College of Cornell University
        • 연락하다:
        • 수석 연구원:
          • Sam Sigal, M.D.
        • 부수사관:
          • Brian P. Bosworth, M.D.
        • 부수사관:
          • Ilan Weisberg, M.D.

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

Phase A Inclusion Criteria:

  • Subject is 18 to 70 years of age, inclusive.
  • Subject has cirrhosis due to chronic HCV infection as documented by:
  • Subject has evidence of hepatic encephalopathy as evidenced by:
  • Neuro-psychometric Testing (Number Connection Test, Trails Test, etc.)
  • Subject is non-azotemic (creatinine <1.5mg/dL) and ambulatory at screening.
  • Subject has cirrhosis due to chronic HCV as documented by: pathologic or clinical and radiographic evidence of cirrhosis with a positive HCV RNA PCR level.

Phase A Exclusion Criteria:

  • Subject has received active interferon therapy within 2 weeks of enrollment.
  • Subject is pregnant or lactating.
  • Subject has a life expectancy of less than 100 days.
  • Subject has a history of alcohol abuse within 6 months of enrollment.
  • Subject has active gastrointestinal bleeding at time of enrollment.
  • Subject has used an agent that alters intestinal motility, eg, methadone, cholestyramine, tricyclic antidepressants.
  • Subject is unable to take oral medication.
  • Subject has used neomycin or other antibiotic within 2 weeks of enrollment or is actively using lactulose at time of enrollment.
  • Subject is taking or has hypersensitivity or allergy to rifaximin or rifampin.
  • Subject requires long term antibiotic therapy (eg, Lyme Disease, tuberculosis).
  • Subject has known or suspected alcohol abuse or illicit drug use within 1 year of enrollment.
  • Subject has participated in an investigational drug or device study within the 30 days prior to randomization.
  • Subject has received rifaximin within the last 30 days.
  • Subject has concomitant disease or condition that could interfere with, or for which treatment could interfere with the conduct of the study, or could in the opinion of the investigator increase the risk of AEs for the subject's participation in the study.
  • Subject is unwilling or unable to comply with the study protocol for any other reason.
  • Subject has been diagnosed with other forms of liver disease, including those with HIV and HBV co-infection, as determined by history, serological parameters, and histology when available.
  • Subject has been diagnosed with a major psychiatric illness, chronic renal and/or respiratory insufficiency, intercurrent infections, treatment with sedatives within 7 days of enrollment.
  • Subject shows presence of intestinal obstruction or inflammatory bowel disease, antacids or cathartics within the 12h before study start; antibiotics during 7 days before start of dosing; or treated with encephalopathy-causing agents.
  • Subjects with bad vision or neurological diseases since they could have difficulty completing the neuropsychological assessments.

Phase B Inclusion Criteria

  • Subject successfully participated in and continues to meet all eligibility criteria required in Phase A of the study based on completion of tests, Breath Tests, and Radiological Marker.
  • Subject has a Number Connection Test score >50 sec at time of enrollment.

Phase B Exclusion Criteria

  • A subject will not be eligible for inclusion in Phase B if (s)he meets any of the exclusion criteria for Phase A of the study.

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: 크로스오버 할당
  • 마스킹: 삼루타

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Phase A: Degree of bacterial overgrowth and its correlation with the grade of hepatic encephalopathy (if present)
기간: 3 months
3 months
Phase B: Improvement in the psychometric scores and proportion of patients who change of HE stage
기간: 3 months
3 months

2차 결과 측정

결과 측정
기간
Improved Intestinal transit time
기간: 3 months
3 months
Improvement in bacterial overgrowth
기간: 3 months
3 months
Improved insomnia
기간: 3 months
3 months
Improved flatulence
기간: 3 months
3 months
Improved quality of life.
기간: 3 months
3 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Sam Sigal, M.D., Weill Medical College of Cornell University

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

2005년 12월 1일

기본 완료 (예상)

2012년 12월 1일

연구 완료 (예상)

2012년 12월 1일

연구 등록 날짜

최초 제출

2006년 1월 20일

QC 기준을 충족하는 최초 제출

2006년 1월 20일

처음 게시됨 (추정)

2006년 1월 24일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2010년 11월 5일

QC 기준을 충족하는 마지막 업데이트 제출

2010년 11월 4일

마지막으로 확인됨

2010년 11월 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. .

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