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Clinical Trials/NCT07674680
NCT07674680RecruitingPhase 1

Beta3-adrenergic Receptors and Cardiovascular Function in Aging Women

University of Missouri-Columbia1 site in 1 country60 target enrollmentStarted: July 31, 2026Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 1
Status
Recruiting
Enrollment
60
Locations
1
Primary Endpoint
Blood flow

Study Overview

Brief Summary

To determine if vascular beta3 adrenergic receptors are present and functional in aging women and can be targeted to attenuate sympathetic vasoconstriction and enhance vascular function in aging women.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Single (Participant)

Eligibility Criteria

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

Inclusion Criteria

  • •Healthy women,
  • •Assigned female at birth,
  • •18-70 years of age,
  • •Body mass index <18 or ≥30 kg/m2,

Exclusion Criteria

  • •Assigned male at birth,
  • •Pregnancy,
  • •Breastfeeding,
  • •History of hormone replacement therapy, chemical menopause, or oophor-ectomy
  • •Polycystic ovarian syndrome or Primary ovarian insufficiency,
  • •Current smoking/Nicotine use,
  • •Blood pressure ≥140/90 mmHg,
  • •Increased risk of bleeding, pro-coagulant disorders, clotting disorders, anticoagulation therapy,
  • •Nerve/neurologic disease,
  • •Cardiovascular, hepatic, renal, respiratory disease,
  • •Hypersensitivity to nitroglycerin,
  • •Diabetes,
  • •Communication barriers,

Arms & Interventions

Cold pressor test

Experimental

Participants will be exposed to the cold pressor test (ice water on the foot).

Intervention: Gemtesa (Drug)

Flow Mediated Dilation

Experimental

Participants will be exposed to the high-resolution ultrasound following inflation of a cuff around the forearm.

Intervention: Placebo (Drug)

Flow Mediated Dilation

Experimental

Participants will be exposed to the high-resolution ultrasound following inflation of a cuff around the forearm.

Intervention: Gemtesa (Drug)

Cold pressor test

Experimental

Participants will be exposed to the cold pressor test (ice water on the foot).

Intervention: Placebo (Drug)

Outcomes

Primary Outcomes

Blood flow

Time Frame: Change from baseline to minute 2.

Blood flow measured with Doppler ultrasound.

Secondary Outcomes

No secondary outcomes reported

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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