Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
Healthy Volunteers
NCT07250217

Determination of Epigenetic Markers of Acute Myeloblastic Leukemia in Elderly Patients

Led by Groupe Hospitalier de la Region de Mulhouse et Sud Alsace · Updated on 2026-02-04

30

Participants Needed

2

Research Sites

98 weeks

Total Duration

On this page

Sponsors

G

Groupe Hospitalier de la Region de Mulhouse et Sud Alsace

Lead Sponsor

I

Institut de Recherche en Hématologie et Transplantation (IRHT)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The main objective of this study is to identify epigenetic markers specific to abnormal myeloid cells in patients with acute myeloid leukemia (AML) by analyzing the methylation of circulating cell-free DNA in plasma.

CONDITIONS

Official Title

Determination of Epigenetic Markers of Acute Myeloblastic Leukemia in Elderly Patients

Who Can Participate

Age: 60Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 60 years or older
  • For control group: scheduled for cardiac surgery involving sternotomy
  • Normal blood count within two months before sampling (control group)
  • Diagnosis of de novo AML or AML secondary to myelodysplastic syndrome, scheduled for azacitidine-based treatment (AML group)
  • Affiliated with or beneficiary of a social security system
  • Written informed consent to participate in the study
Not Eligible

You will not qualify if you...

  • Patients unsuitable for sampling by the surgeon (control group)
  • Patients under legal protection measures
  • Patients under judicial supervision or deprived of liberty by judicial or administrative decision
  • Presence of active infection markers (hepatitis B, hepatitis C, or HIV)
  • Diagnosis of a hematologic disease other than AML (AML group)
  • Clinical signs suggesting active central nervous system leukemia or isolated extramedullary leukemia (AML group)
  • Previous AML treatment other than hydroxyurea (AML group)
  • Severe comorbidities interfering with the study as assessed by the principal investigator (AML group)

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

Groupe Hospitalier de la Région de Mulhouse et Sud Alsace

Mulhouse, Alsace, France, 68100

Actively Recruiting

2

GHRMSA

Mulhouse, France, 68100

Actively Recruiting

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Research Team

B

Bernard DRENOU, Dr

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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