Sympathetic Neurovascular Transduction: Role of Adrenergic Receptors and Sex Differences

Recruiting now · Phase 4

Conditions studied: Vasoconstriction, Vasodilation

In brief

The main purpose of this interventional study is to examine differences in resting blood pressure control between healthy males and females. The main questions it aims to answer are: 1. Are there sex differences in the communication between the sympathetic nervous system (also known as the "fight or flight" response) and peripheral blood vessels (which influence systemic blood pressure)? 2. What is the role of specific vascular receptors that respond to sympathetic signals, and is it different between males and females? Participants will complete one study visit of approximately 3 hours where they will: * Have a blood sample taken to measure circulating sex hormone and sympathetic transmitters. * Receive very small doses of medications commonly used to adjust blood pressure through an artery in their arm. The effects of these medications will be short-acting and localized to the forearm. * Have their sympathetic nervous activity directly measured through two very small needles (similar to acupuncture needles) in the side of their leg. * Have their blood pressure and heart rate recorded, and forearm blood flow measured using ultrasound.

Key facts

Study ID

NCT05997732

Run by

University of Alberta

People needed

30

Starts

2023-10-31

Expected to finish

2027-12-01

Last updated by the study team

2026-01-08

Who can join

Age: 18 and older, up to 40. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Between ages 18-40 years
• No diagnosed medical history of cardiovascular, respiratory, nervous system, or metabolic disease.
• Females must be pre-menopausal.
• Prior to study visit: abstained from caffeine, alcohol, strenuous exercise, and medication not taken regularly for at least 12 hours.

You may not qualify if…

• Current diagnosis of cardiovascular, respiratory, nervous system, or metabolic disease that may impact blood pressure regulation. This will be assessed on a case-by-case basis by the study physician.
• Participants with bleeding or clotting disorders, or those currently taking blood thinners.
• Participants currently taking beta-agonist inhalers i.e. Ventolin (at least not in the last 24 hours).
• Females who are pregnant, confirmed by a pregnancy test.
• Females who have are less than 1 year postpartum or are breastfeeding.
• Females who are post-menopausal.
• Participants that are classified as obese (body mass index > 30 kg ⋅ m2).
• Have a history of smoking regularly in the last 6 months (but nicotine substitutes (i.e. patch, gum) are not an exclusion criteria).
• Those with a known allergy to sulfites, or other components of the supplied solution of study drugs.
• Participants taking medications that are contraindicated with any of the study drugs, such as monoamine oxidase (MAO) inhibitors or tricyclic antidepressants.
• Participants who have not adhered to the pre-testing guidelines related to diet, alcohol or exercise will not be excluded, but will be rescheduled for a different day. This is to reduce experimental variability.

Where it is running

• University of Alberta — Edmonton, Alberta, Canada (enrolling)

Full record on ClinicalTrials.gov

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