PET/CT scan with a new tracer versus ultrasound to detect early psoriatic arthritis
Compares a PET/CT tracer with ultrasound in adults with psoriasis and joint pain.
Key facts
- Who runs it
- UZ Leuven
- Where
- Edegem and Leuven, BelgiumSee the 2 sites
- Trial code
- Registry title
- Prospective diagnostic performance of PET/CT using the novel fibroblast imaging tracer [18F]-AlF-FAPI-74 versus power doppler ultrasound in psoriasis patients with arthralgia: early detection of psoriatic arthritis
- Status
- Not yet recruiting
- Phase
- Phase 2/3
- People taking part
- 270 people, planned
- Started
- 1 Oct 2026
- Expected to end
- 1 Jan 2031
- Type of study
- Interventional
- Record updated
- 16 October 2026
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 and joint pain that has lasted more than 2 weeks but less than 2 years. It compares a PET/CT scan with ultrasound for spotting early psoriatic arthritis.
- Age
- Older than 18 years
- Sex
- Men and women can join. Women must be post-menopausal, surgically sterile, or using effective contraception with a negative pregnancy test.
- Disease stage
- Psoriasis (plaque, guttate or pustular) confirmed by a dermatologist. Ongoing inflammatory joint or tendon-attachment pain for more than 2 weeks but less than 2 years, not caused by injury, with morning stiffness of more than 10 minutes.
- Earlier treatment
- People cannot have started systemic immunosuppressive treatment, including bDMARDs or tDMARDs, before the study scan.
Main reasons for not taking part
- Current or past other inflammatory arthritis
- Pregnancy, breast-feeding or planning pregnancy
- Past or present cancer
- Peripheral joint replacement
- Known allergy to [18F] AlF-FAPI-74 or its ingredients
The registry criteria, word for word
Show all 17 criteriaShow less
Who can take part
- Voluntary written informed consent must be obtained prior to any screening procedures
- Subject is aged > 18 years
- Female subjects should be (a) post-menopausal, or (b) surgically sterile, or (c) using effective contraceptive with negative pregnancy test
- Patients need to have a dermatologist confirmed clinical diagnosis of psoriasis, either plaque psoriasis, guttate psoriasis or pustular
- Patient has persisting (inflammatory) arthralgia of the peripheral joints or entheses for more than 2 weeks, but less than 2 years not caused by trauma and with a morning stiffness of more than 10 minutes
Who cannot take part
- Participation in a clinical scientific trial in the last 12 months with a radiation exposure caused by the experimental procedures greater than 1 mSv
- Use of systemic immunosuppressive therapy, including treatment with bDMARDs or tDMARDS, for psoriasis or another condition already started before study scan
- Current or history of other inflammatory arthritis
- Participant has a known hypersensitivity to [18F] AlF-FAPI-74 or the used excipients
- Diagnosis of other generalized dermatological conditions, such as atopic dermatitis, SLE, ……
- History or presence of malignancy
- Any disorder or condition, which in the Investigator’s opinion might jeopardise the participant’s safety or compliance with the protocol
- Participation in an interventional Trial with an investigational medicinal product (IMP) or device when the trial designs are not considered compatible by the study team
- Contraindication to PET scan (pregnancy, claustrophobia ……)
- Patients with peripheral joint replacement
- Participant is mentally or legally incapacitated, do not understand the trial design or is not willing or capable to undergo all trial-specific procedures
- Female who is pregnant (urinary hCG test will be performed in every WOCBP), breast-feeding or intends to become pregnant or is of child-bearing potential and not using an adequate, highly effective contraceptive (with a relatively high Pearl Index: natural methods, minipill outside postpartum period, spermicides or condoms in monotherapy or no usage of contraception when sexually active are not accepted)
Where in Belgium
- Universitair Ziekenhuis AntwerpenEdegem, BelgiumNot yet recruiting
- UZ LeuvenLeuven, BelgiumNot yet recruiting
About the trial
What the trial wants to find out
Demonstrate that the diagnostic/predictive performance of [18F] AlF-FAPI-74 PET/CT is equivalent or superior to the current gold standard, power doppler ultrasound, for the development of clinical psoriatic arthritis within 2 years (non-inferiority study with non-inferiority limit 10%) in psoriasis patients with arthralgias
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
- Prospective diagnostic performance of PET/CT using the novel fibroblast imaging tracer [18F]-AlF-FAPI-74 versus power doppler ultrasound in psoriasis patients with arthralgia: early detection of psoriatic arthritis
- Plain-language title
- PET/CT scan with a new tracer versus ultrasound to detect early psoriatic arthritisGenerated 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 October 2026