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NCT Number: NCT07047352

Prospective Study Evaluate the Timing of Empirical Treatment for Carbapenem-resistant Bacterials (CROEAT Study)

In this study, we will evaluate the feasibility and clinical outcomes of risk adaptive empirical therapy to cover carbapenem resistance gram negative bacteria (CRO) in patients with hematological malignancies colonized with CRO. Patients assessed by the clinician as being at high risk for CRO infection and requiring intravenous antibiotics covering CRO must meet the following conditions:

1. Positive active screening for CRO or past CRO infection or local prevalence of CRO (e.g.,CRO detection rate>20% among recently hospitalized patients); 2. Presence of fever or other possible signs and symptoms of infection; 3. Neutropenia(ANC<0.1×10^9/L)expected to last for ≥7 days,and having any of the following:

* Gastrointestinal mucositis/peri-anal infection/intestinal obstruction;

* Shock or severe sepsis;

* Respiratory failure:deoxygenated PaO2<60 mmHg or requiring mechanical ventilation;

* Disseminated intravascular coagulation;

* Altered mental status or psychiatric abnormalities;

* Congestive heart failure requiring treatment;

* Arrhythmia requiring treatment;

* Recurrence of fever shortly after cessation of or during empirical treatment with carbapenems (≤7 days).

The endpoints of study include incidence of blood-stream infection by CRO, incidence of all causes mortality, incidences of clinical and microbiology response.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rui Jin Hospital

Shanghai, Shanghai Municipality, 200025, China

Location contact

Jiong HU

CONTACT

[email protected]

86-13764313546

Jiong HU

PRINCIPAL_INVESTIGATOR

Ling wang

CONTACT

About this study

Neutropenic fever is common in patients with hematological malignancies undergoing chemotherapy or transplantation. Empirical antibiotics therapy is essential treatment principle. In China, recent evidence demonstrated that the carbapenem resistant gram negative bacteria was emerging as an important issue and CRO colonization was positive in about 10% of patients by rectal swab. In such group of patients, the empirical treatment of patients with neutropenic fever therapy remained as a challenge. In this study, we plan to evaluate the feasibility and clinical outcomes of risk adaptive empirical therapy to cover CRO in patients with hematological malignancies colonized with CRO.

Patients assessed by the clinician as being at high risk for CRO infection and requiring intravenous antibiotics covering CRO must meet the following conditions:

  • Positive active screening for CRO or past CRO infection or local prevalence of CRO (e.g.,CRO detection rate>20% among recently hospitalized patients);
  • Presence of fever or other possible signs and symptoms of infection;
  • Neutropenia(ANC<0.1×10^9/L)expected to last for ≥7 days,and having any of the following:
  • Gastrointestinal mucositis/peri-anal infection/intestinal obstruction;
  • Shock or severe sepsis;
  • Respiratory failure:deoxygenated PaO2<60 mmHg or requiring mechanical ventilation;
  • Disseminated intravascular coagulation;
  • Altered mental status or psychiatric abnormalities;
  • Congestive heart failure requiring treatment;
  • Arrhythmia requiring treatment;
  • Recurrence of fever shortly after cessation of or during empirical treatment with carbapenems (≤7 days).

The endpoints of study include incidence of blood-stream infection by CRO, incidence of all causes mortality, incidences of clinical and microbiology response.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with hematological malignancies receiving hospital treatment such as chemotherapy/immunotherapy/hematopoietic stem cell transplantation;
  • Those with a recent history of CRO colonization or who have been screened for CRO once a week continuously since admission;
  • Patients assessed by the clinician as being at high risk for CRO infection and requiring intravenous antibiotics covering CRO must meet the following conditions:
  • Positive active screening for CRO or past CRO infection or local prevalence of CRO (e.g.,CRO detection rate>20% among recently hospitalized patients);
  • Presence of fever or other possible signs and symptoms of infection;
  • Neutropenia(ANC<0.1×10^9/L)expected to last for ≥7 days,and having any of the following:
  • Gastrointestinal mucositis/peri-anal infection/intestinal obstruction;
  • Shock or severe sepsis;
  • Respiratory failure:deoxygenated PaO2<60 mmHg or requiring mechanical ventilation;
  • Disseminated intravascular coagulation;
  • Altered mental status or psychiatric abnormalities;
  • Congestive heart failure requiring treatment;
  • Arrhythmia requiring treatment;
  • Recurrence of fever shortly after cessation of or during empirical treatment with carbapenems (≤7 days).
  • The patient or their legal guardian has signed the informed consent form.

Exclusion criteria

  • Pregnant or breastfeeding women;
  • Individuals who are expected to die within 14 days of hospitalization or have an expected hospital stay of less than 7 days;
  • Any conditions that the investigator believes may increase the risk to the patient;
  • Severe psychological or psychiatric disorders with poor estimated compliance;
  • The presence of any other conditions that the investigator deems unsuitable for participation in this study.

Treatment and study plan

Empirical treatment

Other

Empirical treatment to cover carbapenem-resistant enterobacterales

Primary outcomes

  1. Incidence of overall mortality

    Time frame: 14 days

    Patients died of any causes

Secondary outcomes

  1. Incidence of documented CRE blood stream infection

    Time frame: 30 days

    Patients with positive culture of carbapenem-resistant enterobacterales

  2. Clinical response

    Time frame: 14 days

    Patients with full recovery of clinical signs and symptoms of infection

  3. microbiology response

    Time frame: 14 days

    Patients with clearance of blood carbapenem-resistant enterobacterales

Study contacts

Contact information is provided by the study sponsor or research team.

Ling Wang

CONTACT

jiong hu

CONTACT

[email protected]

86-13764313546

Sponsors and collaborators

Lead sponsor

Shanghai Jiao Tong University School of Medicine

Other

Registry information

Official study title

A Multi-center Single Arm Prospective Study in Patients of Hematological Malignancies Colonized With Carbapenem-resistant Bacterials to Evaluate the Timing of Empirical Antibiotic Treatment (CROEAT Study)

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Jul 2, 2025
Registry last updated
Jul 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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