Impact of Early Aging and Menopause on the Vascular Responses to Hypoxia
University of Missouri-Columbia · NCT06417177
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–70 · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Early Phase 1
- Target enrollment
- 75
- US sites recruiting
- 1
- Study start
- June 3, 2024
- Record last updated
- September 10, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this study is to examine hypoxic vasodilation and the role of beta-adrenergic receptors in younger premenopausal, perimenopausal, and older postmenopausal women.
Being studied: Placebo; Propranolol; Gemtesa
Conditions: Aging; Menopause; Hypoxia; Vasodilation
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Female assigned at birth
- Pre, peri- or post-menopausal
- Healthy weight (BMI ≥18 and ≤30 kg/m2)
Exclusion Criteria
- Male (assigned at birth)
- Pregnancy, breastfeeding
- Use of hormone replacement therapies
- Hysterectomy
- Body mass index >30 kg/m2
- Diagnosed sleep apnea
- Current smoking/Nicotine/Drug use
- Nerve/neurologic disease
- Cardiovascular, hepatic, renal, respiratory disease
- Blood pressure ≥140/90 mmHg
- Diabetes, Polycystic ovarian syndrome
- Communication barriers
- Prescription medications
- Malignant cancer
Recruiting US locations
University of Missouri-Columbia
Columbia, MO 65211
Site contact: Jacqueline K Limberg, Ph.D. · 573-882-2420 · limbergj@missouri.edu
Study contacts (from the official record)
- Jacqueline Limberg · 573-882-2544 · limberglab@missouri.edu
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