Actively Recruiting
Biological Bank for Patients with Autoimmune Cytopenia in a Constitutive Reference Center
Led by University Hospital, Bordeaux · Updated on 2025-03-26
200
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University Hospital, Bordeaux
Lead Sponsor
M
Ministry for Health and Solidarity, France
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are conducting an observational study to create a biological bank for patients with autoimmune cytopenia, including immune thrombocytopenia (ITP), autoimmune hemolytic anemia (AHA), autoimmune neutropenia, and erythroblastopenia. This research is a collaboration between clinical departments, biological resource centers, and research units such as CNRS and INSERM. It aims to support future translational and fundamental research to better understand these conditions and develop new treatments. The study involves collecting biological samples including 45 ml of whole blood to isolate peripheral blood mononuclear cells and monocytes, as well as 12 ml of urine. These samples will be used for basic research projects and might also be made available to the pharmaceutical industry to aid in the development of new molecules. The biological bank will support ongoing research into molecular mechanisms involved in platelet formation disorders and the role of regulatory CD8+ T lymphocytes in autoimmune hemolytic anemia. Participants will provide informed consent and biological samples at the start of the study. Researchers will track the number of patients with autoimmune cytopenia who are newly diagnosed or under follow-up but not treated, using their biological samples for analysis. The study includes regular assessments as needed and will continue until 2027. Patient involvement includes sample donation and adherence to study procedures, with the goal of improving understanding and treatment options for autoimmune cytopenia.
CONDITIONS
Brief Title
Biological Bank for the Patients Followed in a Constitutive Reference Center for Autoimmune Cytopenia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients over 16 years old
- Diagnosis of autoimmune cytopenia according to the latest French National Care Protocol (PNDS 2017)
- Affiliated with or beneficiary of a social security scheme
- Provided free, informed, written consent before any research examination
You will not qualify if you...
- Positive for HIV, Hepatitis B, or Hepatitis C virus
- Pregnant or breastfeeding women
- Currently receiving treatment for autoimmune cytopenia
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 5 years
Participants who undergo routine care are observed and biological samples such as blood and urine are collected to support research on autoimmune cytopenia.
Visits occur as part of routine care with biological sample collections as scheduled
Trial Site Locations
Total: 1 location
1
CHU de Bordeaux - service de médecine interne
Pessac, France
Actively Recruiting
Research Team
J
Jean-François VIALLARD, Prof
I
Isabelle RAYMOND, Pharm
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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