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Autonomic Involvement in Patient With Cognitive Decline

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Enrolling

Conditions

Dementia of Alzheimer Type
Dementia, Mild

Treatments

Device: Sudoscan

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Prospective interventional study with a device for comparing autonomic parameters among patients with different forms of cognitive decline

Enrollment

120 estimated patients

Sex

All

Ages

50 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • male and females between 50 and 85 years
  • cognitive decline (dementia, lewy's body dementia, Parkinson dementia, Alzheimer dementia)
  • mild cognitive decline ( lewy's body MCI, Parkinson MCI and Alzheimer MCI)
  • Ability to assume the upright position

Exclusion criteria

  • diabetes mellitus
  • eye problems
  • severe cognitive decline
  • heart disease
  • peripheral neuropathy
  • language barrier
  • oncological disease
  • medical pathologies associated with cognitive deficits

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

120 participants in 1 patient group

cognitive decline
Experimental group
Description:
comparison of autonomic parameters among subjects with different forms of cognitive decline
Treatment:
Device: Sudoscan

Trial contacts and locations

1

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Central trial contact

Camillo Marra, MD

Data sourced from clinicaltrials.gov

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