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RECRUITING
NCT06022016
NA

Study of Families With an Hemopathies Predisposition Related to the DDX41 Gene.

Sponsor: Institut Claudius Regaud

View on ClinicalTrials.gov

Summary

This is a multicenter, interventional, historico-prospective cohort pilot study aimed at specifying the phenotype of subjects carrying a constitutional familial DDX41 mutation, with a view to eventually publishing oncogenetic recommendations for carriers of this mutation. The main objective of the LUCID project is to assess the cumulative risk of hematological diseases as a function of age in DDX41 germline mutation carriers. This study will be carried out in two stages: Stage 1: Inclusion of index cases in an oncogenetic consultation (salivary test, completion of an health self-questionnaire and collection of contact details for the related cases). Stage 2: Proposition of participation to family members, by correspondence, and determination of carrier or non-carrier status of the constitutional familial DDX41 mutation (based on a salivary test). A maximum of 210 index case patients and 700 family member will be included in this study.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

910

Start Date

2023-11-17

Completion Date

2030-01

Last Updated

2025-12-08

Healthy Volunteers

Yes

Interventions

GENETIC

For each person (index case or related) included in this study:

* an health questionnaire will be completed in order to gather information on the participant's medical history and lifestyle. * a saliva sample will be taken (if applicable) so that a genetic analysis can be performed.

Locations (5)

Chu de Bordeaux

Bordeaux, France

Chu de Limoges

Limoges, France

Institut Paoli-Calmettes

Marseille, France

Chu de Montpellier

Montpellier, France

IUCT-O

Toulouse, France