University of Missouri-Columbia
Columbia, Missouri, 65211, United States
NCT Number: NCT05256069
The purpose of this project is to identify sex-related differences in the effect of hypoxia on sympathetic vascular transduction.
Looking for future studies?
Notify Me18 year–45 year
All sexes
Interventional
Early Phase 1
Columbia, Missouri, 65211, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive a β-blockade (propranolol pill, 1 mg/kg dosed based on participant weight).
Participants will receive a placebo in pill form.
Time frame: Change from baseline to 5 minutes
Measured with venous occlusion plethysmography (mL/dL/min)
University of Missouri-Columbia
Other
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.
Published trials that share one or more normalized conditions with this study.
NCT04354051
Aneurysm, Cardiovascular Diseases
Norwich, Norfolk, United Kingdom
View Trial DetailsNCT06417177
Aging, Aneurysm
Columbia, Missouri, United States
View Trial DetailsNCT04436731
Aneurysm, Body Weight
Columbia, Missouri, United States
View Trial DetailsNCT06301880
Aneurysm, Cardiovascular Diseases
Damascus, Syria
View Trial Details