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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02149498
Other study ID # PD-MAG-01
Secondary ID
Status Not yet recruiting
Phase N/A
First received May 26, 2014
Last updated May 26, 2014
Start date July 2014
Est. completion date July 2016

Study information

Verified date April 2014
Source Sheba Medical Center
Contact Naama Warman Alaluf, Msc
Phone 972-3-530-4931
Email naama.warmanalaluf@sheba.health.gov.il
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

A cornerstone in PD research is the investigation of neurophysiological changes as potential biomarkers that could help in tracking disease progression and response to therapies. Electroencephalography (EEG) could provide a non-invasive and relatively cheap tool for identification of such biomarkers. In this study we will use high-density electroencephalograph (EEG) recording, in order to develop a platform of biomarkers that could be more sensitive and reliable to disease progression and response to therapeutic intervention than standard clinical measures.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date July 2016
Est. primary completion date July 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria:

1. Idiopathic PD patients (according to the UK PD Society brain bank clinical diagnostic criteria (bradykinesia plus at least one other cardinal feature of PD, no atypical features or secondary cause) and HC aged 40-80 years

2. PD patients Hoehn and Yahr stages I to IVStable PD therapy

Exclusion Criteria:

- In the investigator's opinion, any unstable or clinically significant condition that would impair the participants' ability to comply with study requirements.

- Patients or HC with significant psychiatric symptoms or history

- BDI score <14

- MMSE <25

- Treatment with neuroleptics.

- For PD patients: Hoehn and Yahr Stage 5

- PD Patients with severe dyskinesia or tremor

- PD Patients with atypical Parkinsonism or secondary Parkinsonism

- History or evidence of neurological problems: cerebrovascular disease, previous head injury or neurosurgical interventions.

- Currently with lice or open wounds on scalp.

- Significant sensory deficits, e.g., deafness or blindness

- Current drug abuse or alcoholism.

- Pregnancy or not using a reliable method of birth control.

- Participation in current clinical study or clinical study within 30 days prior to this study.

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Dr. Oren Cohen

Outcome

Type Measure Description Time frame Safety issue
Primary Functional networks of brain activity in Idiopathic PD patients and healthy individuals measured using analysis of EEG Event Related Potential The study outcome measure are functional networks of brain activity of PD patients and healthy individuals established based on an analysis of EEG data recorded while study subjects perform ERP tasks 2 WEEKS No
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