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TRANSLATE - Lupus Registry

TRANSLATE - Lupus Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00032997
Enrollment
500
Registered
2024-02-05
Start date
2024-10-17
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

M32

Interventions

Group 1: We will included Patients = 18 years, who have been diagnosed with SLE according to the 2019 EULAR / ACR criteria and whoe are able to understand the nature and individual consequences of par

Sponsors

Universitätsklinikum Köln - Klinik II für Innere Medizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. signed informed consent form 2. patients = 18 years of age with a diagnosis of systemic lupus erythematosus according to the EULAR/ ACR criteria of 2019

Exclusion criteria

Exclusion criteria: 1. refusal of participation 2. patients < 18 years

Design outcomes

Primary

MeasureTime frame
As this is clinical registry, no primary endpoint was defined. The aim of the registry is to collect clinical data longitudinally to detect patient characteristics that are associated with a certain outcome of the the disease. This will pave the way for the development of individualized disease management strategies. Furthermore we will collect biomaterial (e.g. blood and urine) to identify novel biomarkers or pathogenic cellular mechanisms.

Secondary

MeasureTime frame
As this is a clinical registry, no secondary outcome was defined.

Countries

Germany

Outcome results

None listed

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