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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05116436
Other study ID # 2019-A03136-51
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 6, 2020
Est. completion date June 6, 2022

Study information

Verified date November 2021
Source Ramsay Générale de Santé
Contact Jean-François Oudet
Phone 0683346567
Email jf.oudet@ecten.eu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 43
Est. completion date June 6, 2022
Est. primary completion date June 6, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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).

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Blood sample
It will test the presence or absence of genetic mutations found in other cohorts in previous studies.
Spine X-ray
To determine the scoliosis

Locations

Country Name City State
France Clinique Maussins-Nollet Paris

Sponsors (2)

Lead Sponsor Collaborator
Ramsay Générale de Santé European Clinical Trial Experts Network

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Presence of a mutated allele in scoliosis patients versus their healthy relatives. 12 months
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