Biological Collection for Marfan and Related Syndromes
ConditionMarfan Syndrome
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age3-99
SponsorUniversity Hospital, Toulouse
About this trial
The present study will establish a collection of biological samples from Marfan patients or with associated diseases 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 Marfan syndrome or related syndromes
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 followed at the Rare Diseases Reference Centre (CRMR) for Marfan syndrome at the Toulouse University Hospital.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
collection of samples of blood and urine
Biological/Vaccineextra samples of blood and urine will be collected and stored for research utilisation
Treatment groups
300 Participants
are divided into 1 treatment groupGroup A: Patients with Marfan syndrome or related syndromes1 intervention
Trial outcomes
Primary outcomes
1
Constitution of a biological collection from patients with Marfan or related syndromes.
extra sample of blood and urine will be collected
Time frame
Day 02
Constitution of a biological collection from patients with Marfan or related syndromes. Collection of samples at inclusion.
extra sample of blood and urine will be collected
Time frame
during the intervention/procedure/surgerySponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov