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Survivin as Predictive Biomarker for RA

Survivin as Predictive Biomarker for Development of Rheumatoid Arthritis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03444623
Acronym
SurviPred
Enrollment
6000
Registered
2018-02-23
Start date
2013-06-30
Completion date
2023-12-31
Last updated
2022-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthralgia, Joint Pain, Rheumatoid Arthritis

Keywords

predictive factor, prognostic factor

Brief summary

Purpose: to examine the possibility of using the onco-protein survivin as a predictive biomarker for identifying individuals at risk of developing rheumatoid arthritis within a cohort of patients seeking treatment for joint pain/stiffness. Secondly, to study survivin as a prognostic marker for joint destruction, refractory and highly active disease in patients with established RA.

Detailed description

The study will analyse survivin levels in a non-selected material within a cohort of patients seeking help at their primary health care for joint pain, stiffness, swelling etc. Patients presenting with such symptoms (not explained by injury or other factors) are suspected to have an arthritic condition such as RA, and are routinely tested for presence of autoantibodies RF and ACPA. In this observational study we add measurement for survivin to the blood analyses of these patients. Information about patients expressing high levels of survivin will be reported to the referring doctor at the primary health care, and for patients not previously having been examined by a rheumatologist this will be offered. The study will be performed at Sahlgrenska university hospital Gothenburg and Umeå university hospital.

Interventions

None listed

Sponsors

Vastra Gotaland Region
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients seeking treatment at the primary health care for problems with their joints (pain, stiffness).

Exclusion criteria

* Patients diagnosed with RA

Design outcomes

Primary

MeasureTime frameDescription
Survivin positive1 yearSurvivin positive: \> 0,45 ng/ml Survivin negative: \< 0,45 ng/ml

Countries

Sweden

Contacts

Primary ContactMaria Bokarewa, MD
maria.bokarewa@rheuma.gu.se

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026