Following adults with systemic sclerosis and collecting samples over time
Collects clinical data and blood, stool and skin samples from adults with systemic sclerosis.
Plain-language title generated from the registry record
Registry title: Prospective Cohort of Patients With Systemic Sclerosis at Brest University Hospital With Biobanking
Key facts
- Where
- Brest, FranceSee the site
Where in France
- CHRU de BrestBrest, FranceTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- University Hospital, Brest
- Trial code
- NCT05532865
- Record updated
- 26 June 2026
- Original description
This study corresponds to a monocentric prospective cohort of adult patients with systemic sclerosis.Read full original descriptionShow less
Prospective Cohort of Patients With Systemic Sclerosis at Brest University Hospital and Constitution of a Biobank
This study corresponds to a monocentric prospective cohort of adult patients with systemic sclerosis.
It will allow the constitution of an organized collection of longitudinal clinical data as well as collection of biological samples, including blood samples, as well as stool sample and skin swab for microbiota analysis.
Inclusion: Major patient with systemic sclerosis defined according to the EULAR 2013 criteria (see Appendix 1); Patient evaluated within the framework of the reference center for rare autoimmune diseases of the CHU of Brest; Patient affiliated to the social security system; Patient having signed a written informed consent.
Exclusion: Hemoglobin (Hb) level < 7g/dl; Minor; Patient under legal protection (guardianship, curatorship); Refusal to participate; Patient unable to consent; Pregnant or breastfeeding woman.