ClinicalTrials.gg
RecruitingNCT06417177Updated Sep 10, 2026

Impact of Early Aging and Menopause on the Vascular Responses to Hypoxia

An Early Phase 1 interventional study of Placebo and Propranolol in Aging, Menopause and Hypoxia, sponsored by University of Missouri-Columbia. Recruiting at 1 site in United States. Open to female participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-10.

Sponsored by University of Missouri-Columbia · Early Phase 1, Interventional, and Basic science

From the registry’s dates

  • Started Jun 2024; still recruiting 2 years 5 months later.
Phase
Early Phase 1
Study type
Interventional
Enrollment
75
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
Female
01

Study summary

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.

02

Conditions studied

  • Aging
  • Menopause
  • Hypoxia
  • Vasodilation

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03

In context

Hypoxia

1,076 studies on the registry are indexed under Hypoxia; 213 are open to participants now.

This study's planned enrollment of 75 is above the median of 45 across 769 interventional studies indexed under Hypoxia.

Browse Hypoxia studies →

Lead sponsor

University of Missouri-Columbia is the lead sponsor of 365 studies on the registry; 69 are open to participants now.

Of its 43 completed or terminated interventional studies of FDA-regulated products, 29 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Female assigned at birth
  • Pre, peri- or
  • Healthy weight ( ≥18 and ≤30 kg/m2)

Exclusion criteria

Exclusion Criteria:

  • Male (assigned at birth)
  • Pregnancy, breastfeeding
  • Use of hormone replacement therapies
  • Hysterectomy
  • >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
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Early Phase 1
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Participant)
Enrollment
75 participants (estimated)

Study arms

  • Experimental
    Hypoxia

    Participants will be exposed to hypoxia (low oxygen air) using a mask.

    Drug: Placebo · Drug: Propranolol · Drug: Gemtesa

  • Experimental
    Cold pressor test

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

    Drug: Placebo · Drug: Propranolol · Drug: Gemtesa

  • Experimental
    Hypercapnia

    Participants will be exposed to hypercapnia (high carbon dioxide air) using a mask.

    Drug: Placebo · Drug: Propranolol · Drug: Gemtesa

Interventions

  • DrugPlacebo

    Participants will receive a placebo in pill form.

  • Participants will receive oral propranolol (1 mg/kg).

  • Participants will receive oral gemtesa (75 mg).

06

What researchers measure

Primary outcomes

  1. Forearm blood flow

    Blood flow in the forearm measured with venous occlusion plethysmography.

    Time frame: Change from baseline to 5 minutes.

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06417177
Responsible party
Jacqueline K Limberg, PhD (Associate Professor, University of Missouri-Columbia) — Principal investigator
First posted
May 16, 2024
Start date
Jun 3, 2024
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Sep 10, 2026

Study contacts

Jacqueline Limberg
Contact
limberglab@missouri.edu
573-882-2544

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drugs tested here: Propranolol · Vibegron

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