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Genetic screening in Parkinson*s Disease in order to identify patients who can participate in clinical trials with new targeted therapies

Genetic screening in Parkinson*s Disease in order to identify patients who can participate in clinical trials with new targeted therapies - GBA1 and LRRK2 screening

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON45734
Enrollment
1000
Registered
2017-04-04
Start date
2017-04-12
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

movement disorder Parkinson's disease

Interventions

None listed

Sponsors

Centre for Human Drug Research
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Signed informed consent prior to any study-mandated procedure; 2. Diagnosis of Parkinson*s Disease, diagnosed by a neurologist; 3. Has the ability to communicate well with the Investigator in the Dutch language and willing to comply with the study restrictions.

Exclusion criteria

Exclusion criteria: N/A

Design outcomes

Primary

MeasureTime frame
Sequence of the GBA1 gene Presence of 7 specific mutations in the LRRK2 gene

Secondary

MeasureTime frame
Database of genotyped PD patients, for future research on PD

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)