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[18F]Fluoride PET-CT in psoriasis patients at risk for developing psoriatic arthritis

[18F]Fluoride PET-CT in psoriasis patients at risk for developing psoriatic arthritis - Pre-PsA PET

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON56612
Enrollment
15
Registered
2023-03-02
Start date
2024-11-21
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

joint inflammation in skin disease psoriasis psoriatic arthritis

Interventions

None listed

Sponsors

Amsterdam UMC
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Psoriasis - >=1 arthralgia and/or enthesiopathy in >=1 location(s) =1 of the following; - Nail psoriasis - First-degree relative with PsA - BSA >=3%

Exclusion criteria

Exclusion criteria: - Other rheumatic disease (such as Axial SpA, RA, SLE, Sjögren) - Osteoarthritis and/or mechanical explanation of the pain in joints and/or tendons - Clinically evident arthritis (and/or tenosynovitis) - Systemic therapy for psoriasis (DMARD, bDMARD) - Treatment with study medication in the past 3 months - Pregnancy or breast-feeding

Design outcomes

Primary

MeasureTime frame
The main study endpoint(s)/parameter(s) are the number of individuals with PET-positive lesions, the distribution of PET-positive lesions and the quantitative [18F]Fluoride uptake in PET-positive lesions.

Secondary

MeasureTime frame
Secondary outcome is the correlation between PET outcome and development of PsA in 2 years follow up.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)