Clinical trial Recruiting at 1 site Observational

Tracking invasive fungal infections after allogeneic hematopoietic stem cell transplant

Official title: Retrospective and Prospective Longitudinal Observational Study on Invasive Fungal Disease After Allogeneic Hematopoietic Stem Cell Transplantation

Run by Peking University People's Hospital · NCT07569055 · Data updated 2026-11-12

We will follow people who had an allogeneic stem cell transplant to see how often serious fungal infections occur and which clinical factors predict them.

More Allogeneic Hematopoietic Stem Cell Transplantation trials

Quick facts

Study typeObservational
SexAll
Enrollment6000 (estimated)
SponsorPeking University People's Hospital
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Beijing, Beijing Municipality)
StatusRecruiting
StartedMarch 15, 2025
Main results expectedMarch 14, 2031
Study endsMarch 14, 2031
Registry record updatedMay 6, 2026
Trial IDNCT07569055 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are patients who underwent allogeneic HSCT at Peking University People's Hospital or the listed collaborating centers since January 1, 2014 and who can be followed for outcome data.

Probably not a fit

Patients who cannot provide reliable follow-up information (for example due to severe mental disorder or loss to follow-up) or who are deemed unsuitable by investigators may not benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a longitudinal cohort following patients who underwent allogeneic hematopoietic stem cell transplantation at Peking University People's Hospital and collaborating centers since January 1, 2014, to document occurrences of invasive fungal disease (IFD). Clinical data, diagnostic results, antifungal prevention and treatment regimens, pathogen types, and outcomes will be collected and analyzed over time. The project aims to describe changing epidemiology, compare pathogen spectra and clinical features, and identify prognostic factors associated with IFD and IFD-related mortality. Findings will be compared with prior multicenter data (such as CAESAR 2.0) to understand trends after changes in prevention and diagnostic practices.

Why it matters

Potential benefit: If successful, this work could help doctors identify transplant recipients at highest risk for invasive fungal infections and guide prevention and early treatment to reduce deaths and complications.

How similar studies have gone: Large cohort efforts such as CAESAR 2.0 have documented one-year incidence, high mortality, and shifts in pathogen patterns after allo-HSCT, but predictive models for individual risk remain limited, so this work builds on prior descriptive findings.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

Since January 1, 2014, patients who underwent allo-HSCT at Peking University People's Hospital and other assistance centers.

Exclusion Criteria:

1. For any reason, such as the occurrence of severe mental disorders, the follow-up information may be unavailable;
2. Patients deemed unsuitable for the study by the researchers.

Where it's running

  • Peking University People's Hospital
    Beijing, Beijing Municipality, China
    Recruiting

Study contacts

  • Principal investigator: Xiao-Hui Zhang, MD — Peking University Institute of Hematology, Peking University People's Hospital
  • Study coordinator: Jin Wu, MD
  • Email: wujin1996@126.com
  • Phone: 086-01088326002

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.