Lipopolysaccharide Metabolism and Identification of Potential Biomarkers Predictive of Graft-versus-host Disease After Allogeneic Stem Cell Transplantation
NCT ID: NCT03918343
Last Updated: 2025-07-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
95 participants
INTERVENTIONAL
2019-09-06
2025-05-23
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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All patients
Blood sample
blood samples (4 times; 14ml per visit)
Interventions
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Blood sample
blood samples (4 times; 14ml per visit)
Eligibility Criteria
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Inclusion Criteria
* Patients eligible for allogeneic hematopoietic cell transplantation from a related or unrelated donor and after myeloablative or non-myeloablative conditioning.
* Regular follow-up in the center
Exclusion Criteria
* Umbilical cord blood transplantation
* Hemoglobin level less than or equal to 8g / dl
* Known chronic inflammatory bowel disease or gastroenteritis at the time of inclusion.
* Chronic enteropathy with Clostridium Difficile
18 Years
85 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de Besancon
OTHER
Responsible Party
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Principal Investigators
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Etienne Daguindau, MD
Role: PRINCIPAL_INVESTIGATOR
CHU Besançon
Locations
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Centre Hospitalier Universitaire de Besançon
Besançon, , France
Centre Hospitalier Universitaire de Nancy
Nancy, , France
Countries
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Other Identifiers
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P/2018/387
Identifier Type: -
Identifier Source: org_study_id
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