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Mapping Functional Networks of Brain Activity (Brain Network Activation, BNA) Based on Analysis of Evoked Response Potential (ERP) Signals for Healthy Controls Evoked Response Potential (ERP) Signals for Healthy Controls and Patients With Parkinson Disease

D

Dr. Oren Cohen

Status

Unknown

Conditions

Parkinson Disease

Study type

Observational

Funder types

Other

Identifiers

NCT02149498
PD-MAG-01

Details and patient eligibility

About

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.

Enrollment

100 estimated patients

Sex

All

Ages

40 to 80 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

100 participants in 2 patient groups

Parkinson Disease (PD)
Description:
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)
Healthy Controls
Description:
Healthy individuals

Trial contacts and locations

0

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Central trial contact

Naama Warman Alaluf, Msc

Data sourced from clinicaltrials.gov

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