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

Genetic Study of Idiopathic Scoliosis in a Cohort of Families

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05116436
Acronym
SCOGEN
Enrollment
43
Registered
2021-11-11
Start date
2020-06-06
Completion date
2022-06-06
Last updated
2021-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Scoliosis Idiopathic

Brief 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.

Interventions

PROCEDUREBlood sample

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

PROCEDURESpine X-ray

To determine the scoliosis

Sponsors

European Clinical Trial Experts Network
CollaboratorOTHER
Ramsay Générale de Santé
Lead SponsorOTHER

Study design

Observational model
FAMILY_BASED
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Inclusion criteria for sick patients: * Presence of idiopathic scoliosis, diagnosed by a clinical examination by an orthopedic doctor and confirmed by the presence of a Cobb angle greater than 10 ° on radiographs of the spine * Signed informed consent * Affiliation to a social security scheme or beneficiary of such a scheme Inclusion criteria for healthy relatives: * Be related to the first or second degree with at least 2 individuals suffering from idiopathic scoliosis, and whose family tree over 3 generations finds at least 3 cases of idiopathic scoliosis * Do not present with scoliosis (clinical examination by an orthopedic doctor and x-rays of the spine). * Affiliation to a social security scheme or beneficiary of such a scheme

Exclusion criteria

Non-inclusion criteria for sick patients: * Be part of one of the following categories of vulnerable people: protected adults, adults unable to express their consent and not subject to a protection measure, pregnant women, parturients and nursing mothers, people deprived of their liberty, people hospitalized without consent, people admitted to a health or social establishment for purposes other than research * Suspicion of scoliosis secondary to clinical examination Non-inclusion criteria for healthy relatives: * Be part of one of the following categories of vulnerable people: protected adults, adults unable to express their consent and not subject to a protection measure, pregnant women, parturients and nursing mothers, people deprived of their liberty, people hospitalized without consent, people admitted to a health or social establishment for purposes other than research * Discovery of scoliosis during research (if scoliosis of an idiopathic nature: patient included in the cohort of patients, if secondary scoliosis: exclusion from the family). All patients : Pregnancy in progress or desired with discontinuation of contraception (contraindication to the realization of x-rays).

Design outcomes

Primary

MeasureTime frame
Presence of a mutated allele in scoliosis patients versus their healthy relatives.12 months

Countries

France

Contacts

Primary ContactJean-François Oudet
jf.oudet@ecten.eu0683346567
Backup ContactMarie-Hélène Barba
mh.barba@ecten.eu

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026