ConditionEhlers-Danlos Syndrome
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche
About this trial
The main aim of this study is to evaluate the effect of cross linking on the elasticity of skin samples from patients with non-vascular Ehlers-Danlos Syndrome (hEDS or cEDS).
Eligibility criteria
Qualifiers
Patient aged 18 or over, having read and signed the consent form for participation in the study
Patient with classic or hypermobile Ehlers-Danlos syndrome
Regularly followed-up at the non-vascular Ehlers-Danlos Syndrome Reference Center at Garches Hospital.
Disqualifiers
Patient under court protection, guardianship or curatorship
Pregnant or breast-feeding patient
Patient not affiliated to the French social security system
Impossibility of giving the subject informed information and/or written informed consent: dementia, psychosis, disturbed consciousness, non-French-speaking patient
Trial design
Treatments tested in this trial
- skin biopsy
Treatment groups
28 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov