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

4. november 2010 oppdatert av: 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.

Studieoversikt

Status

Ukjent

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Forventet)

50

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

  • Forente stater
    • New York
      • New York, New York, Forente stater, 10021
        • Rekruttering
        • New York Presbyterian Hospital: Weill Medical College of Cornell University
        • Ta kontakt med:
        • Hovedetterforsker:
          • Sam Sigal, M.D.
        • Underetterforsker:
          • Brian P. Bosworth, M.D.
        • Underetterforsker:
          • Ilan Weisberg, M.D.

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 75 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Crossover-oppdrag
  • Masking: Trippel

Hva måler studien?

Primære resultatmål

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

Sekundære resultatmål

Resultatmål
Tidsramme
Improved Intestinal transit time
Tidsramme: 3 months
3 months
Improvement in bacterial overgrowth
Tidsramme: 3 months
3 months
Improved insomnia
Tidsramme: 3 months
3 months
Improved flatulence
Tidsramme: 3 months
3 months
Improved quality of life.
Tidsramme: 3 months
3 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Weill Medical College of Cornell University

Samarbeidspartnere

Bausch Health Americas, Inc.

Etterforskere

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

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. desember 2005

Primær fullføring (Forventet)

1. desember 2012

Studiet fullført (Forventet)

1. desember 2012

Datoer for studieregistrering

Først innsendt

20. januar 2006

Først innsendt som oppfylte QC-kriteriene

20. januar 2006

Først lagt ut (Anslag)

24. januar 2006

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

5. november 2010

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. november 2010

Sist bekreftet

1. november 2010

Mer informasjon

Begreper knyttet til denne studien

Nøkkelord

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • Salix-RifaxPSE-BactOvrGrwth-01

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