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Determinants of Changes in Arterial Load Following Exercise

Determinants of Changes in Arterial Load Following Exercise

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05820243
Enrollment
25
Registered
2023-04-19
Start date
2023-05-12
Completion date
2024-09-30
Last updated
2023-11-28

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

Conditions

Post-Exercise Hypotension

Keywords

arterial stiffness, wave reflections, pulsatile load

Brief summary

The goal of this study is to learn about how blood vessel dilation after exercise effects pulse wave reflection and influences the function of the heart in healthy young adults. The main question it aims to answer is: Are post-exercise decreases in reflected pulse waves due to a decrease in the stiffness of large arteries in the leg or an increase in leg blood flow? Participants will exercise on a stationary bicycle at a moderate intensity for 1 hour during two laboratory visits. Participants will take oral antihistamines to block post-exercise dilation at one visit, and they will take placebo pills at the other visit. At both visits, leg blood flow, pulse wave velocity, and heart function will be measured before exercise and for 120-minutes after exercise.

Detailed description

During exercise, blood vessels increase in size to supply muscles with more blood. After exercise, the muscles that had been used release chemicals called histamines that cause the blood vessels to stay dilated even when the muscles no longer need more blood. It takes around 2 hours for the blood vessels to return to normal. This causes blood pressure to be lower than it usually is at rest. This phenomenon delays the return of pressure waves in arteries that are reflected back to the heart resulting in the heart having to work less hard to pump out blood for about 2 hours after exercise. However, it is unknown why the reflected pressure waves return to the heart later. The aim of this study is to determine if this delay is due to the speed of the reflected waves being slowed by large arteries or dilation of small arteries resulting in the reflections originating further from the heart. By giving antihistamines prior to exercise, post-exercise blood vessel dilation of the small arteries will be largely reduced, thus allowing for the determination of which factor causes the reflected waves to return later. Additionally, it is hypothesized that the reduction in work that the heart must perform results in improved contraction and relaxation of the heart. Thus, an additional aim is to determine how post-exercise blood vessel dilation influence heart function. To accomplish these aims, blood flow leaving the left ventricle and femoral blood flow will be measured via Doppler ultrasound. Applanation tonometry will be used to record pulse waves at the carotid, radial, femoral, and dorsalis pedis arteries. These pulse waves will be used to estimate central blood pressure and to determine pulse wave velocity of different arterial segments. Measurements will be made at baseline and for 120 minutes after a bout of moderate intensity aerobic exercise.

Interventions

Participants will complete 1 hour of exercise on a cycle ergometer at the power output that elicits 60% of their peak rate of oxygen consumption (V02peak).

Sponsors

University of Delaware
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Masking description

Antihistamine and placebo treatments will be provided in opaque gel capsules by a member of the research team not involved in data collection or analysis.

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy men and women * sedentary or recreationally active

Exclusion criteria

* history of cardiovascular events or procedures * stage 2 hypertension (BP: ≥140 systolic or ≥90 diastolic) * metabolic syndrome * renal disease * chronic respiratory disease * currently prescribed any cardiovascular medication * current use of erythromycin and/ ketoconazole * current pregnancy or breastfeeding -hormone replacement therapy- * tobacco use * musculoskeletal injury/disorder that would inhibit cycling exercise * body mass index (BMI) \<18.5 or \>35kg/m\^2 * reduced kidney function (estimated glomerular filtration rate\< 90ml/min/1.73 m\^2) * daily use of fexofenadine and/or famotidine

Design outcomes

Primary

MeasureTime frameDescription
Change in lower limb arterial stiffness120 minutes post-exerciseArterial stiffness of the leg will be assessed via measurement of femoral-pedis pulse wave velocity.
Change in leg vascular conductance120 minutes post-exerciseVascular conductance, an index of peripheral vasodilation, will be determined by measuring femoral blood flow via ultrasound and dividing by mean arterial pressure.
Change in left ventricular pulsatile load120 post-exerciseDoppler echocardiography and arterial tonometry will be used to establish left ventricular pressure-flow relations. Wave separation analysis will subsequently be performed to determine the magnitude and timing of reflected pulse waves.

Secondary

MeasureTime frameDescription
Change in left ventricular diastolic function120 minutes post-exerciseEchocardiographic measures of left ventricular diastolic function will be recorded, including mitral annulus tissue velocity and mitral in-flow velocity

Countries

United States

Contacts

Primary ContactDavid Edwards, PhD
dge@udel.edu302-831-3363
Backup ContactJordan Patik, PhD
jpatik@udel.edu5128206387

Outcome results

None listed

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