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MOLyF : Bone Marrow and Follicular Lymphoma

R

Rennes University Hospital

Status

Enrolling

Conditions

Lymphoma, Follicular

Treatments

Other: Sampling

Study type

Interventional

Funder types

Other

Identifiers

NCT06608147
35RC24_9716_MOLyF

Details and patient eligibility

About

This is a prospective single-center study designed to assess potential differences in cell composition between bone marrows of patients with follicular lymphoma and those from control subjects.

Follicular lymphoma is the most common indolent lymphoma. It is characterised by systematic relapses and bone marrow dissemination in 70% of patients at the time of diagnosis.

Although relapses are thought to be related to refractory tumour cells nested in a supportive microenvironment in the bone marrow, the mechanisms involved are poorly understood.

To study the specificities of the bone marrow of patients with follicular lymphoma, It is necessary to compare them with control samples.

This study takes advantage of surgeries involving sternotomies to recover lost bone marrow and establish a bone marrow bank of patients without hematological disease.

This bank will be used to set up control cohorts for other clinical trials involving patients with follicular lymphoma.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Major patient
  • Patient hospitalized in the thoracic, cardiac and vascular surgery department for surgery involving a sternotomy
  • Patient with free, informed, written consent
  • Patient covered by a health insurance scheme

Exclusion criteria

  • History of haematological malignancy or haemogram disturbance
  • Immunomodulating treatment: immunosuppressants, corticoids, antineoplastics
  • Persons covered by articles L. 1121-5 to L. 1121-8 and L. 1122-1-2 of the French Public Health Code (e.g. minors, protected adults, etc.)].

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

Experimental
Experimental group
Treatment:
Other: Sampling

Trial contacts and locations

1

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Central trial contact

Juliette Ferrant, MD; Alexandra Guerrier

Data sourced from clinicaltrials.gov

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