このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

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).

調査の概要

研究の種類

介入

入学 (推定)

60

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Jiancheng Zhang
  • 電話番号:+86-13554105815
  • メール:zhjcheng1@126.com

研究場所

    • Hubei
      • Wuhan、Hubei、中国、460022
        • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
介入なし:Control group
Patients received standard ICU care.
実験的: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
時間枠
Enteral nutrition FI improvement rate
時間枠:24, 48, 72, 96, and 120 hours after study enrollment
24, 48, 72, 96, and 120 hours after study enrollment

二次結果の測定

結果測定
時間枠
Gut microbiota composition as well as α and β diversity measured from rectal swabs by 16S rRNA gene sequencing
時間枠: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
時間枠: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)
時間枠:24-0 hours and 120 hours after study enrollment
24-0 hours and 120 hours after study enrollment
Serum level of citrulline
時間枠: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
時間枠:0, 24, 48, 72, 96, and 120 hours after study enrollment
0, 24, 48, 72, 96, and 120 hours after study enrollment
SOFA score
時間枠: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.)
時間枠: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
時間枠: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
時間枠: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.)
時間枠: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.)
時間枠:0, 24, 48, 72, 96, and 120 hours after study enrollment
0, 24, 48, 72, 96, and 120 hours after study enrollment
ICU mortality
時間枠:Within 28 days after study enrollment
Within 28 days after study enrollment
In-hospital mortality
時間枠:Within 60 days after study enrollment
Within 60 days after study enrollment
28-day all-cause mortality
時間枠:Within 28 days after study enrollment
Within 28 days after study enrollment
90-day all-cause mortality
時間枠:Within 90 days after study enrollment
Within 90 days after study enrollment
90-day readmission rate
時間枠:Within 90 days after study enrollment
Within 90 days after study enrollment
90-day secondary infection rate
時間枠:Within 90 days after study enrollment
Within 90 days after study enrollment

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年10月1日

一次修了 (推定)

2027年4月30日

研究の完了 (推定)

2027年6月30日

試験登録日

最初に提出

2026年6月1日

QC基準を満たした最初の提出物

2026年6月5日

最初の投稿 (実際)

2026年6月11日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月16日

QC基準を満たした最後の更新が送信されました

2026年9月15日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • zjc202402

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する