Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05924074

Ferroptosis Study in SF3B1-mutant Myelodysplastic Syndromes (FerMDS)

Led by University Hospital, Bordeaux · Updated on 2025-03-19

80

Participants Needed

3

Research Sites

101 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Myelodysplastic syndromes (MDS) are clonal diseases of hematopoietic stem cells (HSC) characterized by dysplastic and inefficient hematopoiesis related to excessive progenitor cell death. Ferroptosis is a recently described cell death mechanism and we think that it could be a major player in the pathophysiology of MDS, involved in the cell death that characterizes these diseases and contributing to cytopenias. The study aims to demonstrate that there is a significant activation of this phenomenon in MDS patients compared to a population of subjects without MDS.

CONDITIONS

Official Title

Ferroptosis Study in SF3B1-mutant Myelodysplastic Syndromes (FerMDS)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years or older
  • Affiliated to or benefiting from a social security scheme
  • Signed free, written, and informed consent
  • For MDS patients: sampling at diagnosis according to WHO 2016 criteria
  • Presence of ring sideroblasts on bone marrow smear for MDS patients
  • For MGUS patients: sampling as part of MGUS exploration according to WHO 2016 criteria
Not Eligible

You will not qualify if you...

  • Red blood cell transfusion within 120 days before sample collection
  • Treatment with hematopoietic growth factors (EPO, TPO, G-CSF) within 30 days before collection
  • Conditions affecting systemic iron metabolism such as hemochromatosis, Gaucher disease, ferroportin disease, or porphyria cutanea tarda
  • Under legal protection measures (guardianship, curatorship)
  • Deprived of liberty by judicial or administrative decision
  • Unable to give consent
  • In exclusion period after another study or participated in another interventional drug study within 30 days before entry

AI-Screening

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Trial Site Locations

Total: 3 locations

1

CHU de Bordeaux, Laboratoire d'Hématologie

Pessac, France

Not Yet Recruiting

2

CHU de Bordeaux, Service de Médecine Interne

Pessac, France

Not Yet Recruiting

3

CHU de Bordeaux, Service Hématologie Clinique et Thérapie Cellulaire

Pessac, France

Actively Recruiting

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Research Team

V

Victor-Emmanuel BRETT

CONTACT

C

Charles DUSSIAU

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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