Last updated: December 4, 2020
Sponsor: Odense University Hospital
Overall Status: Completed
Phase
N/A
Condition
Joint Injuries
Psoriasis And Psoriatic Disorders
Psoriatic Arthritis
Treatment
N/AClinical Study ID
NCT03058900
OUH-DC-FLORA-01
Ages 18-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Diagnosis of psoriatic arthritis according to the Classification Criteria forPsoriatic Arthritis (CASPAR criteria).
- Presence of active peripheral psoriatic arthritis defined as ≥ 3 swollen joints.
- Methotrexate (≥ 15mg/week (maximal tolerable dosage)) for a minimum of 3 months priorto study inclusion.
Exclusion
Exclusion Criteria:
- Other inflammatory rheumatic diseases than PsA.
- Current axial disease activity or severe peripheral joint activity demanding immediatechange of treatment or contraindicating placebo treatment for 6 months.
- History of severe MTX toxicity or allergic reactions.
- Current biological treatment and biological treatment within the last 6 months.
- Inflammatory bowel disease, celiac disease, food allergy, or other intestinaldiseases.
- Current cancer or severe chronic infections.
- Pregnant or breastfeeding women.
- Systemic and/or local intra-articular or peritendinous steroid injections within 3months of inclusion.
- Non-MTX DMARD treatment within three months of inclusion.
- Antibiotics within 3 months of inclusion.
- Not wishing to participate or unsuited for project evaluation.
Study Design
Total Participants: 31
Study Start date:
May 16, 2017
Estimated Completion Date:
June 02, 2020
Study Description
Connect with a study center
Dept. of Rheumatology at Odense University Hospital
Odense, 5000
DenmarkSite Not Available
Diagnostic Centre at Silkeborg Regional Hospital
Silkeborg, 8600
DenmarkSite Not Available

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