NCT07251556Not yet recruitingPhase 4
GLP-1 Receptor Agonists in Non-diabetic Patients With Psoriatic Arthritis
Effect of Glucagon-Like Peptide-1 (GLP-1) Receptor Agonists on Subclinical Atherosclerosis in Non-diabetic Patients With Psoriatic Arthritis - a Proof-of-concept Randomized Study
Source: ClinicalTrials.gov · Last updated 2 Dec 2025
Brief summary (registry, in English)
Background Psoriatic arthritis (PsA) patients are at increased risk of cardiovascular disease. Glucagon-Like Peptide-1 (GLP-1) receptor agonists are cardiovascular protective in diabetics. They have also anti-inflammatory properties. It is hypothesized GLP-1 receptor agonists can prevent the progression of atherosclerosis due to the combination of metabolic factors and disease activity control in non-diabetic PsA patients. Objectives To investigate the vascular effects of GLP-1 receptor agonists in PsA patients without diabetes. Their metabolic and anti-inflammatory roles will also be examined. Design and subjects This is a pilot randomized open-labelled trial. We plan to enroll 40 non-diabetic patients with PsA. Participants will be randomized 1:1 to either GLP-1 receptor agonist (semaglutide) or control group. Study instruments Subclinical carotid artherosclerosis is assessed by high-resolution ultrasound. Arterial stiffness is measured using pulse wave velocity by a tonometry system, and augmentation index by the SphygmoCor device. These assessments will be done at baseline and 24 weeks. Drug adversities will also be documented. Anthropometric measurements, sugar metabolism and lipid levels as well as the PsA disease activity will be monitored.
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 40 (estimated)
- First submitted
- 26 Sept 2025
- Start date
- 1 Dec 2025
- Primary completion date
- 1 Jan 2027
- Lead sponsor
- Chinese University of Hong Kong
- Diseases
- Psoriasis, Psoriatic arthritis
- NCT number
- NCT07251556
What you commit to
- Study type: Interventional · Phase 4
- Planned participants: 40
- From 1 Dec 2025 to the primary completion date, 1 Jan 2027
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- have prior therapy with GLP-1 receptor agonists during the last 24 weeks,
- have chronic or previous acute pancreatitis,
Other illness
- have pre-existing diabetes,
- have liver or renal impairment,
- have current malignancy,
Other
- have known or symptoms suggestive of CVD,
- are pregnant, breastfeeding or of childbearing potential, or
- are unable to give written informed consent.
Who the study is looking for
- fulfill the ClASsification criteria for Psoriatic Arthritis,
- are rheumatoid factor negative,
- BMI \>=25 kg/m2,
- are over 18 years old and
- Chinese subjects
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.