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Clinical Trials in France / NCT06259890
Recruiting Not applicable

Influence of Sodium Intake in spondyLoarthriTes

NCT06259890 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-01-30
Last updated
2025-07-09

Condition(s) studied

Spondyloarthritis, AxialArthritis, Psoriatic

Investigational drug(s) / intervention(s)

measurement of salt intake

measurement of salt intake: measurement of salt intake without intervention

Study summary

The aim of the SALT study is to analyze the relationship between dietary sodium intake and disease activity in patients with axial spondyloarthritis (radiographic or non-radiographic) or psoriatic arthritis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * patients with axial spondyloarthritis (radiographic or non-radiographic) or psoriatic arthritis * women who have been menopausal for at least 24 months, surgically sterilized, or, for women of childbearing potentiale, use an effective method of contraception (oral contraceptives, contraceptive injections, intrauterine devices, double-barrier method, contraceptive patches) Exclusion Criteria: * patient treated by cyclosporine, diuretics, angiotensin-converting enzyme inhibitors or angiotensin II receptor antagonists. * current treatment with an anti-IL-17A agent (secukinumab or ixekizumab or bimekizumab or brodalumab) or with an anti-IL23 agent (ustekinumab, guselkumab, risankizumab or tildrakizumab) or previous treatment less than 6 months old. * patients on systemic corticosteroids with corticosteroid therapy \> 10 mg prednisone equivalent * pregnant woman

Primary outcome measure(s)

Trial sites (4)

FacilityCityRegionStatus
CHU Besançon Besançon France Recruiting
CHD Vendée La Roche-sur-Yon France Recruiting
CHU St Etienne Saint-Etienne France Recruiting
Hôpital Nord Franche-Comté Trévenans France Recruiting

More Centre Hospitalier Universitaire de Besancon trials in France

Other trials for the same condition

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 NCT06259890 on ClinicalTrials.gov ↗ ← All trials in France