Clinical Trials in France / NCT05202210
Recruiting
Observational
Constitution of a Biological Collection to Study the Pathophysiology in Noonan Syndrome
NCT05202210 · tracked via the Priya Life Science France tracker
Condition(s) studied
Noonan Syndrome
Investigational drug(s) / intervention(s)
blood and urine sampling: extra sample of blood and urine will be collected
Study 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.
Eligibility
Inclusion Criteria:
* 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 Criteria:
* Patients subject to a legal protection measure (guardianship, curators, or safeguard of justice)
* Pregnant or breastfeeding women
Primary outcome measure(s)
- Constitution of a biological collection from patients with Noonan or related syndromes. — inclusion
extra sample of blood and urine will be collected
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Purpan University Hospital | Toulouse | France | Recruiting |
More University Hospital, Toulouse trials in France
Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05202210 on ClinicalTrials.gov ↗ ← All trials in France