Scan test for early bone changes in people with psoriasis
Tests a fluoride body scan to find early bone changes in adults with psoriasis.
Key facts
- Who runs it
- Stichting Amsterdam UMC
- Where
- Amsterdam, NetherlandsSee the site
- Registry title
- [18F]Fluoride PET-CT in psoriasis patients at risk for developing psoriatic arthritis
- Status
- Recruiting
- Phase
- Phase 2
- People taking part
- 15 people, planned
- Started
- 16 Dec 2024
- Expected to end
- 1 May 2027
- Type of study
- Interventional
- Record updated
- 16 December 2024
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with psoriasis who have recent joint or tendon-attachment pain and may be at risk of developing psoriatic arthritis. They will have a whole-body [18F]Fluoride PET-CT scan.
- Age
- 18 years or older
- Sex
- Women and men can join.
- Disease stage
- Diagnosis of psoriasis, with at least 1 painful joint and/or tendon-attachment problem (arthralgia and/or enthesiopathy) in at least 1 place for 1 year or less, not caused by an injury. Also at least 1 of these: nail psoriasis, a first-degree relative with psoriatic arthritis, and/or psoriasis covering 3% or more of the body surface (BSA ≥3%).
- Earlier treatment
- People who had systemic therapy for psoriasis (DMARD, bDMARD) or study medication in the past 3 months cannot join.
Main reasons for not taking part
- Another rheumatic disease (such as Axial SpA, RA, SLE, Sjögren)
- Osteoarthritis and/or a mechanical cause of the joint or tendon pain
- Clearly visible arthritis (and/or tenosynovitis)
- Systemic therapy for psoriasis (DMARD, bDMARD)
- Pregnancy or breast-feeding
The registry criteria, word for word
Show all 9 criteriaShow less
Who can take part
- Patients with a diagnosis of psoriasis and an age of 18 years or older
- ≥1 arthralgia and/or enthesiopathy in ≥1 location(s) ≤ 1 year, not secondary to trauma
- ≥1 of the following: Nail psoriasis, First-degree relative with PsA and/or BSA ≥3%
Who cannot take part
- Systemic therapy for psoriasis (DMARD, bDMARD)
- Treatment with study medication in the past 3 months
- 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)
- Pregnancy or breast-feeding
Where in Netherlands
- Amsterdam UMC StichtingAmsterdam, NetherlandsTaking people
About the trial
What the trial wants to find out
The primary objective of this proof-of-concept study is to investigate the feasibility of whole body [18F]Fluoride PET-CT scans to detect axial and peripheral new bone formation, in psoriasis patients that are at risk to develop clinically manifest psoriatic arthritis.
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?
Contact the study team: see the registry record
Print a page for my doctorData and sources
- Registry record
- Listed on the EU's official list of trials (CTIS).
- Official title
- [18F]Fluoride PET-CT in psoriasis patients at risk for developing psoriatic arthritis
- Plain-language title
- Scan test for early bone changes in people with psoriasisGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 9 November 2026.
- Record updated
- 16 December 2024