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Assessment of Cholinergic and Cognitive Function Using Pharmacologic ASL-Perfusion MRI

Assessment of Cholinergic and Cognitive Function Using Pharmacologic ASL-Perfusion MRI

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01379001
Enrollment
60
Registered
2011-06-23
Start date
2008-07-31
Completion date
2013-01-31
Last updated
2013-01-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cholinergic Function

Keywords

cholinergic function, aging, pharmacologic MRI

Brief summary

This research study will look at how medications affect the pattern of blood flow in the brain. This study will use a special type of MRI (magnetic resonance imaging) scan called perfusion MRI to make measurements of cerebral (brain) blood flow. The medications we will use in this study are scopolamine (commonly used to treat motion sickness), mecamylamine (used to treat high blood pressure), and donepezil (used to treat memory loss). Cognitive testing will also be obtained, and correlated with the blood flow patterns in the brain.

Detailed description

Project Summary: This research project will investigate the value of combined pharmacologic manipulation and arterial spin-labeled perfusion MRI (pharmacologic ASL-pMRI) as an in vivo probe of cholinergic function. Methods to investigate cholinergic function in vivo are needed to better understand the role of acetylcholine in the physiology of the cerebral cortex, and in cognitive processes in health and in disease states. In this study, pharmacologic ASL-pMRI will be used to characterize the normal cerebral perfusion response to cholinergic manipulation in young healthy subjects. Cognitive measures will also be obtained and correlated with cerebral perfusion changes. Pharmacologic ASL-pMRI and cognitive testing will then be used to study how the cholinergic response is altered with normal aging and in delirium

Interventions

DRUGScopolamine

Scopolamine 0.4mg IM x 1 dose; adjustment in older group for weight (0.4mg/70kg)

DRUGPlacebo

IM or PO placebo

DRUGDonepezil

donepezil 5mg PO x 1

Sponsors

Hebrew SeniorLife
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
21 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy volunteers

Exclusion criteria

* Any neurological condition, such as brain tumor, history of stroke, seizure disorder, attention deficit disorder, normal pressure hydrocephalus, dementia, traumatic brain injury * Any major medical conditions, such a cancer, diabetes, glaucoma, prostate disease, uncontrolled hypertension * antihistamine use * tricyclic antidepressant use * presence of metal in body, including pacemaker, defibrillator, neurostimulator, metal implants, or foreign metal objects such as bullets or shrapnel. * anxiety or panic disorder * history of claustrophobia * pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Cerebral blood flow3 hourscerebral blood flow will be measured 3 hours after drug administration using Arterial spin-labeled perfusion MRI

Secondary

MeasureTime frameDescription
cognitive performance4 hoursparticipants will undergo cognitive testing following drug administration and MRI acquisition

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026