M06 M45 M34 M07
Conditions
Interventions
Group 1: Patients with the diagnosis spondylarthritis: One time testing through quantitative sensory Testing including a questionnaire on the clinical manifestation of the disease
Group 2: Patients wi
Sponsors
Universitätsklinikum Bonn
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Person in the age range of 18-65 years Confirmed diagnosis of the following underlying rheumatological disease: - Rheumatoid arthritis according to the 2010 Amercian College of Rheumatology (ACR) criteria. - Systemic sclerosis according to the 2013 ACR/EULAR classification criteria. - Ankylosing spondylitis according to the ASAS criteria - Psoriatic arthritis according to the 2010 American College of Rheumatology (ACR) criteria. Prior informed consent and informed written consent.
Exclusion criteria
Exclusion criteria: Inability to give informed and written consent. Contraindications to the use of QST: - Skin and soft tissue diseases. - Pregnancy - Nursing Period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Detection of deviations in the pain profile/somatosensory profile by means of a one-time testing using quantitative sensory testing (QST) in patients with rheumatoid arthritis (rheumatoid arthritis, psoriatic arthritis, systemic sclerosis, spondylarthritis). | — |
Secondary
| Measure | Time frame |
|---|---|
| Recording of the relation between individual parameters of the QST and information in the questionnaire on disease activity, medication, laboratory parameters and organ manifestation. | — |
Countries
Germany
Contacts
Public ContactRuth Schrapper
Universitätsklinikum Bonn
Outcome results
None listed