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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03021031
Other study ID # NEURO-2016-25066
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date September 19, 2017
Est. completion date January 2027

Study information

Verified date June 2023
Source University of Minnesota
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The goal of this project is to provide comprehensive longitudinal assessments of a cohort of PD patients before, during, and after DBS surgery, including neurological, neurophysiological, and neuropsychological data.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 60
Est. completion date January 2027
Est. primary completion date July 1, 2026
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: - Age 21 years and older - Diagnosis of Parkinson's disease - Candidate for DBS Exclusion Criteria: - Diagnosis of dementia - Pregnant women

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Observational
Observational study

Locations

Country Name City State
United States University of Minnesota Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
University of Minnesota

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Registry This is a registry of patients undergoing DBS surgery. The goal of this project is to provide comprehensive longitudinal assessments of a cohort of PD patients before, during, and after DBS surgery, including neurological, neurophysiological, and neuropsychological data. 5 Years
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