Constitution of a Biological Collection to Study the Pathophysiology in Noonan Syndrome
ConditionNoonan Syndrome
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-99
SponsorUniversity Hospital, Toulouse
About this trial
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 criteria
This trial does not accept healthy volunteersQualifiers
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)
Disqualifiers
Patients subject to a legal protection measure (guardianship, curators, or safeguard of justice)
Pregnant or breastfeeding women
Trial population
Patients with Noonan syndrome
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
blood and urine sampling
Biological/Vaccineextra sample of blood and urine will be collected
Treatment groups
100 Participants
are divided into 1 treatment groupGroup A: patients with Noonan syndrome1 intervention
Trial outcomes
Primary outcomes
1
Constitution of a biological collection from patients with Noonan or related syndromes.
extra sample of blood and urine will be collected
Time frame
inclusionSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov