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Genetic Analysis of Childhood Obesity

NCT02326480 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2020-03-03

No results posted yet for this study

Summary

Identify news genetic causes of different type of obesity (syndromic, familial or isolated obesity) by highlighting new mutations or new implied genes

Conditions

Interventions

OTHER

Identification of genetic causes of obesity

A blood test will be performed to the child and his/her parents with the aim of identifying genetic causes of obesity. Different analysis will be as follows: caryotypes, Raindance, whole exome, in order to find potential mutations or new genes associated to this condition

Sponsors & Collaborators

  • Institut Pasteur de Lille

    collaborator OTHER

  • Lille Catholic University

    lead OTHER

Principal Investigators

  • Louise Montagne · Groupement des Hôpitaux de l'Institut Catholique de Lille

  • Philippe Froguel, MD, PhD · UMR CNRS 8199, Institut Pasteur de Lille

Eligibility

Min Age
6 Months
Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2020-12-31
Completion
2021-06-30

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

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 NCT02326480 on ClinicalTrials.gov