Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT07348471

Fecal Microbiota Transplantation for the Treatment of ICU Delirium

Led by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Updated on 2026-04-03

60

Participants Needed

1

Research Sites

145 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Delirium in the intensive care unit (ICU) is a prevalent and serious neurological complication among critically ill patients, with large multicenter studies reporting an incidence of 30% to 80%, particularly in those requiring mechanical ventilation. Delirium is not only associated with prolonged ICU and hospital stays but also with increased morbidity and mortality. Notably, up to 40% of survivors suffer from persistent cognitive dysfunction that may last for months or even years. Despite current standard pharmacological interventions-such as haloperidol and second-generation antipsychotics-failing to demonstrate significant clinical benefit in phase III trials, non-pharmacological strategies remain challenging to implement due to environmental and operational constraints within the ICU. This unmet clinical need underscores the imperative to develop novel, effective therapeutic approaches. Emerging evidence suggests that ICU-acquired gut microbiota dysbiosis plays a pivotal role in the pathogenesis of delirium. Dysbiosis can compromise intestinal barrier integrity, promoting systemic inflammation and increasing susceptibility to various forms of delirium, including acute illness-related and postoperative types. These effects are likely mediated through the "gut-microbiota-brain axis," which may represent a central mechanism underlying neurocognitive dysfunction in critical illness. Preclinical studies have demonstrated that fecal microbiota transplantation (FMT) can restore microbial balance and exert beneficial effects on neurological function. FMT has shown promise in ameliorating cognitive deficits in models of Alzheimer's disease, chronic cerebral hypoperfusion, traumatic brain injury, and chronic unpredictable mild stress (CUMS). Clinically, FMT has been associated with cognitive improvement in patients with dementia, recurrent Clostridioides difficile infection, and sepsis-associated encephalopathy. With expanding applications in both gastrointestinal and extraintestinal disorders, FMT has emerged as a transformative therapeutic modality, supported by robust short- and long-term safety and efficacy data. This study aims to evaluate whether FMT can alleviate delirium severity, correct gut microbiota dysbiosis at 0, 72, and 120 hours post-enrollment, attenuate intestinal barrier dysfunction, reduce systemic inflammation and disease severity, shorten ICU length of stay, and lower rates of ICU mortality, in-hospital mortality, and 28-day all-cause mortality-ultimately positioning FMT as a potential breakthrough intervention for ICU delirium.

CONDITIONS

Official Title

Fecal Microbiota Transplantation for the Treatment of ICU Delirium

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Positive CAM-ICU delirium diagnosis
  • Expected ICU stay of 5 days or more after enrollment
  • Signed written informed consent
Not Eligible

You will not qualify if you...

  • Routine daily use of antipsychotic medications before ICU admission
  • Severe systemic infection, hemodynamic instability, or serious electrolyte/acid-base imbalance
  • High risk of death within 5 days or treatment limitations
  • Active major gastrointestinal bleeding, perforation, or severe intestinal damage
  • Inability to tolerate at least 50% of calorie needs by enteral nutrition due to severe gastrointestinal issues
  • Planned or recent abdominal surgery within 14 days
  • Current diagnosis of fulminant colitis or toxic megacolon
  • Recent high-risk immunosuppressive or cytotoxic treatments (e.g., rituximab, doxorubicin, or high-dose corticosteroids for over 4 weeks)
  • Pregnancy or lactation
  • Participation in another clinical trial within the past 3 months
  • Inability to reliably assess delirium due to language barriers, sensory impairments, or coma
  • Doubtful validity of informed consent due to mental illness, intellectual disability, or poor motivation

AI-Screening

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Trial Site Locations

Total: 1 location

1

Department of Critical Care Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, China

Actively Recruiting

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Research Team

J

Jiancheng Zhang

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

2

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