Skip to content

Effects of multimodal rheumatologic complex treatment for 16 days - a monocentric prospective study

Effects of multimodal rheumatologic complex treatment for 16 days - a monocentric prospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00021261
Enrollment
120
Registered
2020-04-06
Start date
2018-01-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Degenerative disorders like gonarhrosis patients with Primary fibromyalgia every Patient treated with MRCT at our centre M06.90 M45.00 M35 L40.5

Interventions

Group 1: patients treated with MRCT in our centre

Sponsors

Campus Kerckhoff der Justus-Liebig-Universität Gießen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: patient, who are treated with MRCT classification criteria of disease need to be fulfilled

Exclusion criteria

Exclusion criteria: missing written study consent

Design outcomes

Primary

MeasureTime frame
Change in pain levels measured by a numeric rating scale (0-10) before and after a 16 day MRCT period

Secondary

MeasureTime frame
Change before and after a 16 day MRCT period - functional health (FFbH, HAQ, BASFI) - disease activity (DAS28, BASDAI, WOMAC, AUSCAN, FIQ) - Cytokinlevels of IL10, TNF, IL6, IL17, IL1 Change before MRCT and 12 weeks after discharge: - functional health (FFbH, HAQ, BASFI) - disease activity (DAS28, BASDAI, WOMAC, AUSCAN, FIQ) - Cytokinlevels of IL10, TNF, IL6, IL17, IL1 Change after MRCT and 12 weeks after discharge - functional health (FFbH, HAQ, BASFI) - disease activity (DAS28, BASDAI, WOMAC, AUSCAN, FIQ) - Cytokinlevels of IL10, TNF, IL6, IL17, IL1

Countries

Germany

Contacts

Public ContactPhilipp Klemm

Campus Kerckhoff der Justus Liebig Universität Giessen, Abt. für Rheumatologie, Immunologie, Osteologie und Physikalische Medizin

p.klemm@kerckhoff-klinik.de06032-996-2101

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026