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NCT07188909

Clinical Observation on the Efficacy of Patient-Donor Derived Probiotics in Improving Intestinal Flora Disorder in Patients With Intestinal Acute Graft-Versus-Host Disease (aGVHD)

Not yet recruiting NA Last updated 23 September 2025
What this trial tests

NA trial testing Patient-Donor Derived Probiotics in Acute Graft-Versus-Host Disease in 10 participants. Not yet recruiting.

Timeline
15 September 2025
Primary endpoint
4 March 2026
4 March 2026

Quick facts

Lead sponsorInstitute of Hematology & Blood Diseases Hospital, China
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment10
Start date15 September 2025
Primary completion4 March 2026
Estimated completion4 March 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Institute of Hematology & Blood Diseases Hospital, China

Who can join

50 and older, any sex, with Acute Graft-Versus-Host Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To clinically evaluate the efficacy of patient- and/or donor-derived probiotics in ameliorating intestinal flora dysbiosis in patients with acute intestinal graft-versus-host disease (aGVHD), thereby mechanistically enhancing clinical outcomes and quality of life through intestinal microbiome modulation.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Institute of Hematology & Blood Diseases Hospital, China trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07188909.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing