ClinicalTrials.Veeva

Menu

Effects of Antihypertensive Drug Treatment on Brain Blood Flow, Cognition, and Regulation of Nervous System in Older Adults With Hypertension.

The University of Texas System (UT) logo

The University of Texas System (UT)

Status and phase

Invitation-only
Early Phase 1

Conditions

Older Adults
Essential Hypertension

Treatments

Drug: chlorthalidone
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT06287580
STU-2024-0140

Details and patient eligibility

About

High blood pressure (BP) is a public health problem worldwide. Nearly three-quarters of older adults (age ~60 years) in the United States have high BP. High BP links to many health problems, like stroke. Drug treatments are typically used in clinics to reduce high BP and the risk of associated health problems. However, these drug treatments may not always benefit brain health. For example, drug treatment may reduce brain blood flow, which may reduce cognitive function in older adults with high BP. Alternatively, reduced brain blood flow may cause high BP due to increased nervous system activity (the so-called "fight or flight response"). Thus, monitoring brain blood flow may help to manage high BP during drug treatment.

It is unknown if brain blood flow and its control will be altered by drug treatment in older high BP patients. Therefore, study team will recruit older adults with high BP, who receive either drug treatment or a placebo for 1 to 2 weeks and will assess brain blood flow, cognitive function, and nervous system control before and after treatment.

Results from this study will provide novel and clinically relevant information on the impact of drug treatment for high BP on brain health. Investigators expect these results will suggest that it is crucial to measure brain blood flow, which may be a therapeutic new target for BP control and brain health.

Enrollment

50 estimated patients

Sex

All

Ages

60 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Older men and women with prehypertension or mild-to-moderate essential hypertension (clinic systolic blood pressure 120-169 and/or diastolic blood pressure 80-109 mmHg).

Exclusion criteria

  • Any evidence of cardiovascular or pulmonary disease by medical history or by physical examination
  • Severe hypertension (systolic BP ≥170 and/or diastolic BP ≥110 mmHg; for safety reasons) or secondary hypertension
  • Being on ≥3 antihypertensive agents
  • Chronic kidney disease (an estimated glomerular filtration rate >45 mL/min) or renal failure
  • Diabetes mellitus (fasting glucose ≥126 mg/dL or 2-hour oral glucose tolerance test, glucose level ≥200 mg/dL) or other systemic illness
  • Any history of substance abuse (other than tobacco)
  • Current cigarette smokers
  • History of gouty arthritis
  • Taking hormonal replacement therapy
  • Endurance-trained athletes
  • Diagnosed Alzheimer's disease and related dementias

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

50 participants in 2 patient groups, including a placebo group

Antihypertensive drug treatment Arm
Active Comparator group
Description:
Participants will take a fixed dose of chlorthalidone (a diuretic, 12.5 mg or 25 mg orally once daily) for one to two week, with study visits for laboratory assessment at before and after intervention.
Treatment:
Drug: chlorthalidone
Placebo treatment Arm
Placebo Comparator group
Description:
Participants will receive placebo treatment for one to two weeks, with study visits for laboratory assessment at before and after intervention.
Treatment:
Other: Placebo

Trial contacts and locations

1

Loading...

Central trial contact

TAKURO WASHIO, Ph.D.; Qi Fu, Ph.D.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems