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Brain Blood Vessel Responses to Changes in Blood Flow: Younger Cohort

Cerebrovascular Responses to Acute Hypoperfusion

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06629090
Enrollment
36
Registered
2024-10-08
Start date
2025-12-17
Completion date
2027-05-01
Last updated
2026-07-06

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

Conditions

Cerebrovascular Circulation, Magnetic Resonance Imaging

Keywords

Magnetic Resonance Imaging, Brain Blood Flow, Lower Body Negative Pressure, Carbon Dioxide

Brief summary

Brain blood flow will be measured during a simulated postural change test and while breathing increased levels of carbon dioxide using magnetic resonance imaging.

Detailed description

Global cerebral blood flow (CBF) decreases with advancing age; however, some adults have accelerated declines in CBF, placing them at a greater risk of cognitive impairment. However, there is a lack of human studies that investigate the cause or consequence of altered blood flow regulation in the brain. This study will systematically address this gap in knowledge by examining cerebrovascular control in adults during acute physiological challenges (simulated postural change test and breathing increased carbon dioxide) that stimulate a change in CBF.

Interventions

DEVICEMRI

Participants will undergo an MRI scan while performing breathing and simulated postural change tasks.

DRUGPrazosin

A dose of prazosin will be administered based on body weight

DRUGPlacebo

Oral placebo

Sponsors

University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Between the ages of 20-40 years * Have a BMI ≤34.5 kg/m2 * are less than 72 in (182.88 cm) height * Nonsmoker

Exclusion criteria

* Diagnosis of Mild Cognitive Impairment (MCI) or Alzheimer's disease (AD) * History or evidence of hepatic disease, hematological disease, or peripheral vascular disease; severe kidney injury requiring hemodialysis * History of cardiovascular disease including: severe congestive heart failure, coronary artery disease, ischemic heart disease (stents, coronary artery bypass grafts) and tachycardia * Uncontrolled hypertension * History of clinically significant ischemic or hemorrhagic stroke, or significant cerebrovascular disease * Severe untreated obstructive sleep apnea * History of diabetes with HbA1c greater than 9.5 percent * Major neurologic disorders other than dementia (e.g., MS, ALS, brain surgery, etc.) * Current or recent (less than1 year) major psychiatric condition (Axis I) or addictive disorders * Significant surgical history * Other significant medical conditions at investigators' discretion * Contraindications to MRI * Prescribed medications that interfere with prazosin * Lactose allergy * lower body will not fit in lower body negative pressure (LBNP) chamber (regardless of overall height and BMI)

Design outcomes

Primary

MeasureTime frameDescription
Change in blood velocityTwo study visits, up to 240 minutesThe change in blood velocity during breathing and simulated postural change tasks will be measured with MRI
Change in blood flowTwo study visits, up to 240 minutesThe change in intracranial blood flow during breathing and simulated postural change tasks will be measured with MRI

Countries

United States

Contacts

CONTACTAnna Howery
ahowery@wisc.edu608-262-9572
PRINCIPAL_INVESTIGATORJill Barnes, PhD

UW Madison

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 7, 2026