Actively Recruiting

Age: 18Years +
All Genders
NCT07106931

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Diakonhjemmet Hospital

Oslo, Norway, 0319

Actively Recruiting

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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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