Actively Recruiting
Early STratification of Acute ARThritis
Led by Diakonhjemmet Hospital · Updated on 2025-08-06
400
Participants Needed
1
Research Sites
1051 weeks
Total Duration
On this page
Sponsors
D
Diakonhjemmet Hospital
Lead Sponsor
O
Oslo University Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The prospective observational study "Early STratification of acute inflammatory ARThritis" (START) aims to build a platform for identification of markers for early stratification of inflammatory arthritis to ensure timely diagnosis and correct initial treatment. Management of early-stage inflammatory arthritis is a daily challenge for the rheumatologist and encompasses a range of conditions. Stratification is needed both for optimal diagnostics and for personalising therapy, but is hampered by a lack of tools. Current evaluation is inadequate for early diagnosis and treatment of inflammatory joint diseases as well as for timely diagnosis of infections. The clinical role of novel biomarkers needs to be investigated in large patient samples. In the START study, an extensive data collection will be performed to build a platform for identification and validation of biomarkers for stratification of early-stage inflammatory arthritis. The study has an ambitious goal of improving patient care by increased understanding of the disease. The project applies a unique multitude of approaches to characterisation of patients, including modern imaging techniques, analyses of synovial fluid and -biopsies, genetic and epigenetic markers, proteomics, microbiota analyses and immunological markers. The results will enable clinicians to make better informed treatment decisions for the individual patient with early-stage inflammatory arthritis.
CONDITIONS
Official Title
Early STratification of Acute ARThritis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Arthritis in one or more joints lasting less than 12 weeks
- Adult patients over 18 years old capable of understanding and signing informed consent
- Active clinical synovitis (swelling) in at least one joint confirmed by expert assessment or ultrasonography
- Prior patient-reported swollen joint not confirmed by a rheumatologist is allowed
You will not qualify if you...
- Swollen joint caused by trauma
- Inability to adhere to the study protocol
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Diakonhjemmet Hospital
Oslo, Norway, 0319
Actively Recruiting
Research Team
S
Silje W Syversen, MD PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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