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Recruiting Observational

Biological Collection for Marfan and Related Syndromes

NCT04970459 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2022-01-24
Last updated
2026-03-17

Condition(s) studied

Marfan Syndrome

Investigational drug(s) / intervention(s)

collection of samples of blood and urine

collection of samples of blood and urine: extra samples of blood and urine will be collected and stored for research utilisation

Study summary

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

Sex
ALL
Min age
3 Years
Max age
99 Years
Healthy volunteers
No
Inclusion Criteria: * 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) 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 Marfan or related syndromes. — Day 0
    extra sample of blood and urine will be collected
  • Constitution of a biological collection from patients with Marfan or related syndromes. Collection of samples at inclusion. — during the intervention/procedure/surgery
    extra sample of blood and urine will be collected

Trial sites (1)

FacilityCityRegionStatus
Purpan University Hospital Toulouse France Recruiting
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 NCT04970459 on ClinicalTrials.gov ↗ ← All trials in France