Ireland
--:--IST
Recruiting Not applicable

Autonomic Involvement in Patient With Cognitive Decline

NCT06292741 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2023-01-11
Last updated
2026-09-02

Condition(s) studied

Dementia, MildDementia of Alzheimer Type

Investigational drug(s) / intervention(s)

Sudoscan

Sudoscan: recording of sudomotor function and pupillary reactivity

Study summary

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

Eligibility

Sex
ALL
Min age
50 Years
Max age
85 Years
Healthy volunteers
No
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

Primary outcome measure(s)

  • evaluation of the prevalence in autonomic dysfunction in patients with MCI and dementia — baseline through study completion, an average of 3 year
    evaluation of the prevalence in autonomic dysfunction in patients with MCI and dementia

Trial sites (1)

FacilityCityRegionStatus
Clinica della memria- Fondazione Policlinico Agostino Gemelli IRCCS Rome Lazio Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06292741 on ClinicalTrials.gov ↗ ← All trials in Italy