Status:
RECRUITING
Constitution of a Biological Collection to Study the Pathophysiology in Noonan Syndrome
Lead Sponsor:
University Hospital, Toulouse
Conditions:
Noonan Syndrome
Eligibility:
All Genders
18-99 years
Brief Summary
The present study will establish a collection of biological samples from Noonan patients to be used for research purposes only, with due respect for confidentiality.
Detailed Description
Noonan syndrome is a rare autosomal dominant genetic disorder characterized by a combination of typical facial features, heart defects, short stature, skeletal abnormalities, mild developmental delay ...
Eligibility Criteria
Inclusion
- Children aged at least 3 years old or adult with Noonan syndrome
- Patients affiliated to or beneficiaries of a social security scheme
- Patients able to receive information on the progress of the study and understand the information form to participate in the study. That implies to master the French language and not to be subject to a restriction of rights by the judicial authorities
- Patients or legal representative who have given their consent to participate in the study (expression of no objection)
Exclusion
- Patients subject to a legal protection measure (guardianship, curators, or safeguard of justice)
- Pregnant or breastfeeding women
Key Trial Info
Start Date :
January 26 2022
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
January 26 2032
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT05202210
Start Date
January 26 2022
End Date
January 26 2032
Last Update
December 11 2024
Active Locations (1)
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1
Purpan University Hospital
Toulouse, France, 31059