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COsegregation of VARiants in Panel of Genes

NCT01689584 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11000

Last updated 2026-05-27

No results posted yet for this study

Summary

The aim of the COVAR project is to achieve reliable classification of as many variants of interest as possible from the French OncoGenetics Database (FrOG, https://frog-db.fr/) in order to use them for the genetic counseling. The results obtained through this study will have a major impact on clinical management of the patients and their families conducting in some cases to propose a prophylactic surgery.

Conditions

  • Gene Mutation-Related Cancer
  • Genetic Predisposition

Interventions

GENETIC

salivary kit

The saliva samples will be made of selected related (DNA).

Sponsors & Collaborators

  • Institut Curie

    lead OTHER

Principal Investigators

  • Chrystelle COLAS, MD, PhD · Institut Curie

  • Sandrine CAPUTO, PhD · Institut Curie

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-07-02
Primary Completion
2037-07-02
Completion
2038-01-02

Countries

  • France
  • Guadeloupe
  • Martinique
  • New Caledonia
  • Reunion

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01689584 on ClinicalTrials.gov