IA Trial Radar | ||
|---|---|---|
L'essai clinique NCT06594107 (EISPA) pour Spondyloarthrite axiale est en recrutement. Consultez la vue en carte du Radar des Essais Cliniques et les outils de découverte par IA pour tous les détails, ou posez vos questions ici. | ||
Factors for the Onset and Course of Axial Spondylitis (EISPA)
The purpose of the research project is include newly diagnosed treatment-naive patients with axial spondyloarthritis, to follow them after 1 and 2 years after treatment start, to collect clinical data, questionnaires, blood and urinsamples to find blood or urine markers that can be used for precision therapy of axial spondylitis.
Despite the fact that the disease is relatively common, it takes on average 10 years after start of symptoms for patients be diagnosed with axial spondylitis.
Axial spondylitis diagnosis is based on clinical findings rather than diagnostic tests, which reflects lack of knowledge about what causes the disease. At present, our possibilities to predict the course of the disease (and thereby individualize the care of the patient) are limited. Current treatment decreases inflammation rather than treating the cause of the disease.
The first treatment step of axial spondylitis is with non-steroidal anti-inflammatory drugs or COX inhibitors, which usually have insufficient effect against inflammatory pain and stiffness. In addition, these drugs are associated with side effects, such as gastrointestinal and cardiovascular side effects. Axial spondylitis is a multifactorial disease where the arachidonic acid cascade, an increased prostaglandin production and release may play a major role. With this there is a clear potential to develop new specific drugs to slow down the prostaglandin cascade in patients with axial spondylitis.
Faktorer För Uppkomst Och Förlopp Av Axial Spondylartrit
- EISPA
- 2022-01789-01 (Autre Identifiant) (Karolinska Institute and University Hospital)
axial spondyloarthritis
prostaglandins
predictive factors
| Groupe de participants/Bras | Intervention/Traitement |
|---|---|
1 cohort at Karolinska University Hospital and 1 at the Center for Rheumatology in Stockholm This cohortstudy is performed at 2 sites. | N/A |
| Critères d'évaluation | Description de critères | Période |
|---|---|---|
Prostaglandin levels | Investigators measure prostaglandin levels in treatment-naïve patients at baseline, and then after therapy start after 1 and 2 years. | 2 years |
| Critères d'évaluation | Description de critères | Période |
|---|---|---|
Questionnaires | Investigators collect data on modifiable environmental factors and lifestyle that may contribute to the onset of the disease. | 2 years |
Clinical data | Investigators collect clinical data as entered in the Swedish Rheumatology Quality Register (SRQ) plus the ASAS-health index (0-17, with a lower score indicating a better health status), such as inflammatory markers ESR (mm/hour)/CRP (mg/l), and other variables in the ASAS core outcome set for all trials as defined by ASAS-Omeract. | 2 years |
- newly diagnosed patients with axial spondyloarthritis
- treatment-naive
- 18 years of age or older
- Swedish-speaking
- Able to give informed consent
- DMARD treatment,
- ongoing infection
- ongoing malignancy
Stockholm County