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Clinical Trials/NCT06787066
NCT06787066
Recruiting
Early Phase 1

Sympathetic Vascular Transduction Across the Menopause Transition: Contributing Mechanisms

University of Missouri-Columbia1 site in 1 country75 target enrollmentStarted: July 10, 2025Last updated:

Overview

Phase
Early Phase 1
Status
Recruiting
Enrollment
75
Locations
1
Primary Endpoint
Sympathetic transduction

Overview

Brief Summary

The investigators aim to assess the interactions between the sympathetic nervous system and the vasculature in women across the menopause transition to better understand why aging women have a higher risk of cardiovascular disease.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Assigned female at birth
  • 18-70 years of age
  • Body mass index (BMI) \<30 kg/m2

Exclusion Criteria

  • Assigned male at birth
  • Pregnancy, breastfeeding
  • Body mass index ≥30 kg/m2
  • Oral hormonal contraception in last 6 months, history of hormone replacement therapy, oophorectomy
  • Current smoking/nicotine use
  • Increased risk of bleeding, pro-coagulant disorders, clotting disorders, anticoagulation therapy
  • Nerve/neurologic disease
  • Cardiovascular, hepatic, renal, respiratory disease
  • Blood pressure ≥140/90 mmHg
  • Diabetes, Polycystic ovarian syndrome

Arms & Interventions

Women

Other

Women ages 18-70 years will participate.

Intervention: Propranolol Hydrochloride (Drug)

Women

Other

Women ages 18-70 years will participate.

Intervention: Phentolamine Injection (Drug)

Outcomes

Primary Outcomes

Sympathetic transduction

Time Frame: 1 day (single study visit)

Assessing the relative change in blood flow (Doppler ultrasound) following an increase in sympathetic nerve activity.

Secondary Outcomes

  • Blood flow(1 day (single study visit))
  • Muscle sympathetic nerve activity(1 day (single study visit))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jacqueline K Limberg, PhD

Associate Professor

University of Missouri-Columbia

Study Sites (1)

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