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Central clinical database of the Collaborative Research Centre's INF/ S02 project (CRC/TRR295) "ReTune" to integrate the clinical core dataset

Central clinical database of the Collaborative Research Centre's INF/ S02 project (CRC/TRR295) "ReTune" to integrate the clinical core dataset

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00031878
Enrollment
1012
Registered
2023-05-12
Start date
2023-04-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Patients with movement disorders Parkinson's disease,tremor, dystonia (G20-G26)

Interventions

Group 1: As part of usual care: Implantation of deep brain stimulation device Group 2: As part of usual care: No treatment with deep brain stimulation, because patients refuse this treatment.

Sponsors

Charité Universitätsmedizin Berlin / Klinik für Neurologie mit Experimenteller Neurologie Sektion Bewegungsstörungen und Neuromodulation
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients are eligible for inclusion who: #1 Have been included in a corresponding study of a subproject of TR 295 and have consented to data transfer to the central clinical database as part of inclusion in the respective study. OR #2 Patients with movement disorders Parkinson's disease, tremor, dystonia (G20-G26: Extrapyramidal diseases and movement disorders) who are receiving DBS treatment as part of their therapy and who have consented to inclusion in the central clinical database. OR #3 Patient:s with movement disorders Parkinson's disease, tremor, dystonia (G20-G26: Extrapyramidal diseases and movement disorders) who are eligible for DBS treatment as part of their therapy but have not opted for DBS treatment and have consented to inclusion in the central clinical database (control group).

Exclusion criteria

Exclusion criteria: No signed informed consent form / inclusion criteria are not met

Design outcomes

Primary

MeasureTime frame
Quality of life (EQ-5D-5L) Baseline = t0 / Follow-up = 12 months Occurrence of complications/adverse events

Secondary

MeasureTime frame
Not specified

Countries

Germany

Contacts

Public ContactTRR 295 Coordinator

Charité – Universitätsmedizin Berlin

trr295@charite.de+49(0)30 450 560 373

Outcome results

None listed

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