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DZNE-GBA study: markers in GBA-associated Parkinson disease

DZNE-GBA study: markers in GBA-associated Parkinson disease - MIGAP

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00010156
Enrollment
600
Registered
2016-03-21
Start date
2014-09-29
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

G20

Interventions

Group 1: healthy individuals without Glucocerebrosidase (GBA) mutations: clinical-neurological examination, UPDRS III+IV, BDI-II, NPI-Q, MoCA, TMT, UMSARS 9-12, NMS-Q, Compass31, olfactory performance

Sponsors

DZNE
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 90 Years

Inclusion criteria

Inclusion criteria: - Ability and willingness to communicate comprehensible with the study physician, as well as to understand the demands of the study and to comply with them. - Sign a written consent form for the participation in the study. - Understanding, that a withdrawal of the study participation is possible at any time without negative effects concerning continuation of medical treatment. - manifesting Parkinson disease according to UKBB criteria or no manifesting Parkinson disease according to UKBB criteria.

Exclusion criteria

Exclusion criteria: - Any restriction that hinder the patient to give his consent or comply with any demands of the study. - Other neurodegenerative diseases that make it impossible for the patient to communicate in an adequate way with the study physician or comply with the demands of the study or understand them. - Manifesting dementia according to ICD10. - Occurred cerebral ischemia or cerebral bleeding.

Design outcomes

Primary

MeasureTime frame
- Identification and analysis of factors that cause the disease in GBA carriers or prevent it. - Identiciation of individuals that will develop Parkinson disease because of GBA mutations in the earliest possible stage and examination of these early stages. - Improvement of the knowledge about similarities and differences between Parkinson patients with and without GBA mutation.

Secondary

MeasureTime frame
Identification of specific biomarkers in blood, CSF and cell models

Countries

Germany

Contacts

Public ContactNicole Vollmer

DZNE

n.vollmer@med.uni-tuebingen.de070712985660

Outcome results

None listed

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