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Genetic Study of Idiopathic Scoliosis in a Cohort of Families (SCOGEN)

NCT05116436 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 43

Last updated 2021-11-11

No results posted yet for this study

Summary

This study will focus on a large cohort of multiplex families, to precisely identify candidate genes. The fact of have a large database (fifty families, collected by the principal investigator for more than two decades), will contribute to the discovery of genes of interest. It will also allow testing for the presence or absence of mutations found in other cohorts in previous studies. The main objective of this study is to identify genetic abnormalities associated with the presence and severity of idiopathic scoliosis, in families of scoliosis.

Conditions

  • Scoliosis Idiopathic

Interventions

PROCEDURE

Blood sample

It will test the presence or absence of genetic mutations found in other cohorts in previous studies.

PROCEDURE

Spine X-ray

To determine the scoliosis

Sponsors & Collaborators

  • European Clinical Trial Experts Network

    collaborator OTHER

  • Ramsay Générale de Santé

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-06-06
Primary Completion
2021-06-06
Completion
2022-06-06

Countries

  • France

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 NCT05116436 on ClinicalTrials.gov