| Registry | NCT06520982 |
|---|---|
| Status | Recruiting |
| Phase | Early Phase 1 |
| Study type | Interventional; na, single group, masking: none, basic science |
| Enrollment | 64 (Estimated) |
| Sponsor | University of Missouri-Columbia (Other); collaborators: American Heart Association |
| Conditions | Women, Sympathetic Nervous System, Aging, Blood Flow |
| Interventions | Norepinephrine, Isoproterenol, Acetylcholine, Nitroprusside, Estrogen (Drug) |
| Dates | start 2024-09-20, primary completion 2027-06-30 (estimated), completion 2028-06-30 (estimated), first posted 2024-07-25, last updated 2025-11-26 |
| Locations | 1 site in United States |
Related Papers Related Patents Related Grants Related Experts
All trials for Women All trials for Sympathetic Nervous System All trials of Norepinephrine All trials of Isoproterenol
Our goal is to enhance our understanding of early vascular adaptations in aging women with an emphasis on the sympathetic nervous system.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Women | Other | Drug: Norepinephrine; Drug: Isoproterenol; Drug: Acetylcholine; Drug: Nitroprusside; Drug: Estrogen | Women will be 18-70 years of age |
Sex: Female, ages: 18 Years to 70 Years, accepts healthy volunteers
Inclusion Criteria: * Assigned female at birth (AFAB) * 18-70 years of age Exclusion Criteria: * Assigned male at birth (AMAB) * Pregnancy, breastfeeding * Body mass index ≥30 kg/m2 * Taking medications known to affect metabolic, autonomic, and/or respiratory function * Oral hormonal contraception in last 6 month * History of hormone replacement therapy * History of hyster- or oophor-ectomy * Current smoking/Nicotine use * Increased risk of bleeding, pro-coagulant disorders, clotting disorders, anticoagulation therapy * Chronic disease * Blood pressure ≥140/90 mmHg * Communication barriers
| Facility | City | Country | Status |
|---|---|---|---|
| University of Missouri-Columbia | Columbia, Missouri | United States | Recruiting |