Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
300 participants
OBSERVATIONAL
2022-01-24
2031-08-07
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients with Marfan syndrome or related syndromes
Children aged at least 3 years old or adult with Marfan syndrome or related syndromes
collection of samples of blood and urine
extra samples of blood and urine will be collected and stored for research utilisation
Interventions
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collection of samples of blood and urine
extra samples of blood and urine will be collected and stored for research utilisation
Eligibility Criteria
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Inclusion Criteria
* 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
* Pregnant or breastfeeding women
3 Years
99 Years
ALL
No
Sponsors
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University Hospital, Toulouse
OTHER
Responsible Party
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Principal Investigators
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Thomas Edouard, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Toulouse
Locations
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Purpan University Hospital
Toulouse, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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RC31/21/0178
Identifier Type: -
Identifier Source: org_study_id
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