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EGESTA - Emergent GI Therapy for Severe, Complicated CDI Using Fecal Microbiota Transplant (EGESTA)

22. november 2017 opdateret af: David B. Stewart, MD, FACS, FASCRS, Milton S. Hershey Medical Center

EGESTA - Emergent GI Therapy for Severe, Complicated CDI Using Fecal Microbiota

The objectives/specific aims of this study are three-fold. First, the study seeks to evaluate the safety of fecal microbiota transplant (FMT) in patients with severe, complicated C. difficile infection (scCDI). Second, the study seeks to evaluate whether fecal microbiota transplant (FMT) can improve scCDI, with "improve" defined as either decreasing the severity of CDI, or by resolving the infection altogether. Third, the study seeks to further study the mechanism by which FMT improves the course of scCDI by performing 16S rRNA and ITS sequencing on pre-FMT and serial post-FMT stool samples in order to measure changes to bacterial and fungal microbiota as a consequence of CDI and FMT therapy. FMT material (hereafter referred to as FMTm) would be obtained from OpenBiome. FMTm is prepared from prescreened healthy donors.

The hypothesis of the study is that FMT is a preferred salvage therapy for scCDI as compared to (1) ongoing, failing medical therapy with conventional antibiotics and (2) surgery.

Studieoversigt

Status

Trukket tilbage

Betingelser

Detaljeret beskrivelse

The objectives/specific aims of this study are three-fold. First, the study seeks to evaluate the safety of fecal microbiota transplant (FMT) in patients with severe, complicated C. difficile infection (scCDI). Second, the study seeks to evaluate whether fecal microbiota transplant (FMT) can improve scCDI, with "improve" defined as either decreasing the severity of CDI, or by resolving the infection altogether. Third, the study seeks to further study the mechanism by which FMT improves the course of scCDI by performing 16S rRNA and ITS sequencing on pre-FMT and serial post-FMT stool samples in order to measure changes to bacterial and fungal microbiota as a consequence of CDI and FMT therapy. FMT material (hereafter referred to as FMTm) would be obtained from OpenBiome. FMTm is prepared from prescreened healthy donors.

The hypothesis of the study is that FMT is a preferred salvage therapy for scCDI as compared to (1) ongoing, failing medical therapy with conventional antibiotics and (2) surgery.

The standard of care treatment for scCDI is conventional antibiotics with either parenteral/oral metronidazole, and/or vancomycin provided in the form of oral and/or retention enemas. The reliability of these conventional antibiotics in the setting of scCDI is very unpredictable, and patients with CDI of this severity have a mortality rate that in some series is greater than 50%. It is against the mediocre historical record of these antibiotics that FMT would be tested in this highly moribund patient population.

FMT would not be provided to patients with scCDI off protocol.

Undersøgelsestype

Interventionel

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Pennsylvania
      • Hershey, Pennsylvania, Forenede Stater, 17078
        • David Stewart

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 75 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Adults between 18 years of age and 75 years of age.
  • Have CDI defined as clinical symptoms of CDI (diarrhea with or without abdominal pain/abdominal distention) with a confirmatory nucleic acid amplification test (NAAT) positive for CDI.
  • Have severe/complicated disease as defined by ACG guidelines(appendix 1), with any of the following attributable to CDI:

    • Admission to intensive care unit for CDI
    • Hypotension (systolic blood pressure < 90 mmHg) with or without required use of vasopressors
    • Fever ≥ 38.5 ° C
    • Ileus (as defined by the absence of intestinal function for at least 24 hours and/or radiographic evidence of pathologically dilated small intestine without evidence of a mechanical obstruction) or significant abdominal distention
    • Mental status changes
    • WBC ≥ 35,000 cells / mm 3 or < 2,000 cells / mm 3
    • Serum lactate levels >2.2 mmol / l
    • End organ failure (mechanical ventilation,renal failure as defined by a rise in creatinine of >1.5 mg/dL either above the upper limit of normal for creatinine, or > 1.5 mg/dL from premorbid levels if that information is known, acute hepatic dysfunction as defined by an increase in AST or ALT to twice the upper limit of normal, etc.)

Exclusion Criteria:

  • Pregnant or lactating women
  • Prisoners
  • Patients under the age of 18 or over the age of 76 years of age
  • Patients who are immunocompromised including but not limited to:

    • Have HIV infection historically reported, regardless of CD4 count
    • AIDS as defined by either an AIDS-defining diagnosis (appendix 2) or a CD4 count <200/mm3,
    • Inherited or primary immune disorders,
    • Received chemotherapy within the previous 90 days, or
    • Current or recent treatment with any immunosuppressant medications in the past 90 days
  • Individuals who have received FMT at any time before potential study enrollment
  • Patients who do not have a stool test confirming C. difficile infection
  • Patients who have a severe anaphylactic response to food
  • Patients with allergies to sodium chloride or glycerol, both ingredients Generally Recognized As Safe (GRAS)
  • Patients who have colorectal cancer
  • Diagnosis of Irritable Bowel Disease or Irritable Bowel Syndrome
  • Any other condition for which the Principal Investigator thinks the treatment may pose a health risk
  • Anticipated or predicted death within the time period of follow-up for reasons unrelated to CDI
  • An APACHE II score >29 at the time of evaluation for inclusion in the study protocol (Appendix 4.0)
  • Mandatory ongoing antibiotic use for non-CDI infection
  • Patients unable to provide informed consent or who do not have a legally authorized representative for consent
  • Patients unable to comply with requirements of this study protocol

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: fecal microbiota transplant
250 mL of fecal transplant material by enema as treatment
Fecal microbiota transplant for the treatment of severe, complicated C. difficile infection
Andre navne:
  • FMT Microbiota Preparation

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Safety - adverse events
Tidsramme: Thirty days after treatment
Absence of unexpected related adverse events
Thirty days after treatment

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Efficacy (Cure of infection, or decrease in severity of infection based on white blood cell count)
Tidsramme: Thirty days after treatment
Cure of infection, or decrease in severity of infection based on white blood cell count
Thirty days after treatment

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Samarbejdspartnere

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

15. september 2016

Primær færdiggørelse (Faktiske)

14. november 2017

Studieafslutning (Faktiske)

14. november 2017

Datoer for studieregistrering

Først indsendt

11. november 2016

Først indsendt, der opfyldte QC-kriterier

17. november 2016

Først opslået (Skøn)

18. november 2016

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

27. november 2017

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

22. november 2017

Sidst verificeret

1. november 2017

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • STUDY00005388

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

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