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NCT Number: NCT07242391

Menopausal Hormone Therapy And Left Ventricular Function

The purpose of this study is to compare left ventricular stroke volume and heart rate responses to bursts of SNA between PMF using, and not using, MHT.

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Key information

Age range

45 year–60 year

Sex eligibility

Female

Study type

Observational

Primary location

Mayo Clinic in Rochester

Rochester, Minnesota, 55905, United States

Location contact

Joshua Bock, PhD

CONTACT

[email protected]

(507) 422-0768

Joshua Bock, PhD

PRINCIPAL_INVESTIGATOR

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • >45-60< years of age

Exclusion criteria

  • Male sex
  • Females between STRAW+10 stages -5 and 0
  • PMF in STRAW+10 stage +2
  • PMF using oral hormone therapy
  • Females who entered menopause due to a surgical procedure or in response to pharmacotherapy (e.g., gonadotrophin releasing hormone agonists or chemotherapy)
  • Heart disease such as hypertropic cardiomyopathy, congenital abnormalities, chronic heart failure, valve disease, and a history of myocardial infarction
  • Medications that impact the central nervous system including selective serotonin reuptake inhibitors, anxiolytics, sedatives, anticholinergic agents, dopamine, amphetamines, or wake-promoting agents (e.g., modafinil). Other medications will be evaluated on an individual basis by the PI.
  • Cardiovascular medications is also an exclusion criterion which includes those acting on the renin-angiotensin-aldosterone axis, adrenergic receptor antagonists, diuretics, nitrates, and calcium channel antagonists. Other medications will be evaluated on an individual basis by the PI.
  • Pregnancy
  • COPD
  • Diabetes
  • CKD
  • Raynaud's phenomenon
  • Sleep disorders
  • Shift workers
  • BMI ≥40.0kg/m2
  • Use of nicotine-containing products within the two years preceding study visits
  • Active cancer treatment

Treatment and study plan

Menopausal hormone therapy

Drug

Taken in accordance with standard clinical practice, administered for a minimum duration of eight weeks.

Primary outcomes

  1. Left ventricular stroke volume

    Time frame: Baseline

    Left ventricular stroke volume is the amount of blood pumped from the left ventricle per heartbeat (mL)

Secondary outcomes

  1. Ventriculo-Arterial (VA) coupling

    Time frame: Baseline

    Ventriculo-Arterial (VA) coupling will be measured as the ratio of end-systolic elastance (Ees) to arterial elastance (Ea).

Study contacts

Contact information is provided by the study sponsor or research team.

Joshua Bock, Ph.D.

CONTACT

[email protected]

507-422-0768

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Official study title

Menopausal Hormone Therapy And Neural Control Of Left Ventricular Function

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Nov 21, 2025
Registry last updated
Apr 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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