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FMT for Feeding Intolerance Due to Gastrointestinal Dysfunction in Critically Ill Patients (FMT-FIT)

Fecal Microbiota Transplantation for Feeding Intolerance Due to Gastrointestinal Dysfunction in Critically Ill Patients: A Single-Center, Single-Blind, Randomized Controlled Trial

Critically ill patients admitted to the intensive care unit (ICU) frequently present with gastrointestinal dysfunction and are at elevated risk of malnutrition. Gastrointestinal dysfunction is correlated with adverse clinical outcomes, including prolonged mechanical ventilation duration, extended ICU length of stay, and increased 90-day mortality.

In critically ill ICU patients, severe gut microbiota dysbiosis and intestinal barrier impairment may occur due to the burden of primary critical illnesses, as well as the administration of proton pump inhibitors and antibiotics. This cascade contributes to a high prevalence of gastrointestinal dysfunction, alongside profound gut-derived systemic inflammatory responses and organ damage. Given the pivotal role of gut microbiota in maintaining intestinal homeostasis, fecal microbiota transplantation (FMT) holds promise as a novel therapeutic strategy for enteral feeding intolerance secondary to gastrointestinal dysfunction in critically ill ICU patients.

This study intends to deliver FMT via a nasojejunal tube to critically ill patients with gastrointestinal dysfunction admitted to the ICU. Its objectives are to evaluate the intervention's effects on gastrointestinal function recovery and the alleviation of enteral feeding intolerance, while also assessing its impacts on intestinal barrier function, gut microbiota composition and metabolic profiles, serum metabolite signatures, immune-inflammatory responses (including lymphocyte subsets, cytokines, C-reactive protein, and procalcitonin), ICU delirium, ICU sleep quality, and clinical outcomes (encompassing ICU mortality, in-hospital mortality, 28-day all-cause mortality, 90-day all-cause mortality, 90-day readmission rate, and 90-day incidence of secondary infections).

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

60

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiekontakt

Studiesteder

    • Hubei
      • Wuhan, Hubei, Kina, 460022
        • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
        • Ta kontakt med:

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

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  1. Aged 18 to 70 years inclusive, regardless of ethnicity or gender;
  2. Female participants are either non-fertile (i.e., physiologically incapable of pregnancy, including women with ≥2 years of menopause) or have no pregnancy plans;
  3. Have been admitted to the ICU for ≥24 hours;
  4. Expected ICU stay ≥7 days after study enrollment;
  5. Screened positive for ≥1 manifestation of gastrointestinal dysfunction (intra-abdominal hypertension [IAH], massive gastric retention, diarrhea, lower gastrointestinal paralysis, bowel dilatation); enteral nutrition is then implemented under the guidance of the enteral feeding intolerance (FI) score, and participants with persistent FI after a 3-day trial are formally enrolled;
  6. Participants can actively cooperate or passively complete relevant examinations and follow-up procedures;
  7. Have signed a written informed consent form.

Exclusion Criteria:

  1. Severe systemic infection in the early resuscitation phase, with hemodynamic instability, insufficient tissue perfusion, or severe fluid-electrolyte and acid-base imbalances;
  2. Patients assessed by clinicians as having a high risk of death within 5 days, or those with restricted treatment decisions;
  3. Active gastrointestinal bleeding, perforation, or other conditions with severe intestinal barrier impairment;
  4. Patients unable to tolerate enteral nutrition meeting 50% of caloric requirements due to severe diarrhea, significant fibrotic intestinal stenosis, massive gastrointestinal bleeding, or high-output enterocutaneous fistula;
  5. Planned or recent abdominal surgery (within 14 days prior to enrollment);
  6. Current diagnosis of fulminant colitis or toxic megacolon;
  7. Neutropenia (neutrophil count < 1500 cells/µL);
  8. Patients with congenital or acquired immunodeficiency disorders;
  9. Recent receipt of high-risk immunosuppressive or cytotoxic agents, e.g., rituximab, doxorubicin, or medium-to-high-dose corticosteroids (≥ 20 mg/day prednisone equivalent) for a duration of > 4 weeks;
  10. Pregnant or lactating women;
  11. Participation in another clinical trial as a subject at the time of enrollment or within 3 months prior to enrollment;
  12. Doubtful validity of informed consent: subjects with mental illness, intellectual disability, poor motivation, or other factors that restrict the validity of informed consent for participation in this 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: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Ingen inngripen: Control group
Patients received standard ICU care.
Eksperimentell: FMT intervention group
Patients received FMT via a nasojejunal tube in addition to standard ICU care. Specifically, 50-100 mL of intestinal microbiota suspension was administered daily via the nasojejunal tube between 11:00 and 13:00 for three consecutive days.
Patients received FMT via a nasojejunal tube in addition to standard ICU care. Specifically, 50-100 mL of intestinal microbiota suspension was administered daily via the nasojejunal tube between 11:00 and 13:00 for three consecutive days.

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Enteral nutrition FI improvement rate
Tidsramme: 24, 48, 72, 96, and 120 hours after study enrollment
24, 48, 72, 96, and 120 hours after study enrollment

Sekundære resultatmål

Resultatmål
Tidsramme
Gut microbiota composition as well as α and β diversity measured from rectal swabs by 16S rRNA gene sequencing
Tidsramme: 24-0 hours and 120 hours after study enrollment
24-0 hours and 120 hours after study enrollment
Fecal metabolite profile (by untargeted LC-MS) from rectal swabs
Tidsramme: 24-0 hours and 120 hours after study enrollment
24-0 hours and 120 hours after study enrollment
Serum metabolite profile (by untargeted LC-MS)
Tidsramme: 24-0 hours and 120 hours after study enrollment
24-0 hours and 120 hours after study enrollment
Serum level of citrulline
Tidsramme: 0, 24, 48, 72, 96, and 120 hours after study enrollment
0, 24, 48, 72, 96, and 120 hours after study enrollment
APACHE II score
Tidsramme: 0, 24, 48, 72, 96, and 120 hours after study enrollment
0, 24, 48, 72, 96, and 120 hours after study enrollment
SOFA score
Tidsramme: 0, 24, 48, 72, 96, and 120 hours after study enrollment
0, 24, 48, 72, 96, and 120 hours after study enrollment
Cumulative intravenous dose of vasopressor agents (including norepinephrine, epinephrine, dobutamine, etc.)
Tidsramme: 0, 24, 48, 72, 96, and 120 hours after study enrollment
0, 24, 48, 72, 96, and 120 hours after study enrollment
Serum level of C-reactive protein
Tidsramme: 0, 24, 48, 72, 96, and 120 hours after study enrollment
0, 24, 48, 72, 96, and 120 hours after study enrollment
Serum level of procalcitonin
Tidsramme: 0, 24, 48, 72, 96, and 120 hours after study enrollment
0, 24, 48, 72, 96, and 120 hours after study enrollment
Peripheral blood level of cytokines (including IL-6, IL-17, TNF-α, IL-10, IL-1β, etc.)
Tidsramme: 0 and 120 hours after study enrollment
0 and 120 hours after study enrollment
Peripheral blood lymphocyte subsets (including CD4+ T, CD8+ T, B lymphocytes, NK cells, etc.)
Tidsramme: 0, 24, 48, 72, 96, and 120 hours after study enrollment
0, 24, 48, 72, 96, and 120 hours after study enrollment
ICU mortality
Tidsramme: Within 28 days after study enrollment
Within 28 days after study enrollment
In-hospital mortality
Tidsramme: Within 60 days after study enrollment
Within 60 days after study enrollment
28-day all-cause mortality
Tidsramme: Within 28 days after study enrollment
Within 28 days after study enrollment
90-day all-cause mortality
Tidsramme: Within 90 days after study enrollment
Within 90 days after study enrollment
90-day readmission rate
Tidsramme: Within 90 days after study enrollment
Within 90 days after study enrollment
90-day secondary infection rate
Tidsramme: Within 90 days after study enrollment
Within 90 days after study enrollment

Samarbeidspartnere og etterforskere

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

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 (Antatt)

1. oktober 2026

Primær fullføring (Antatt)

30. april 2027

Studiet fullført (Antatt)

30. juni 2027

Datoer for studieregistrering

Først innsendt

1. juni 2026

Først innsendt som oppfylte QC-kriteriene

5. juni 2026

Først lagt ut (Faktiske)

11. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

16. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

15. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • zjc202402

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-deling Støtteinformasjonstype

  • STUDY_PROTOCOL

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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