Actively Recruiting
Hemodynamics Monitoring During Lower Body Negative Pressure Induced Controlled Hypovolemia
Led by Yale University · Updated on 2026-01-20
120
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research focuses on healthy volunteers aged 20 to 45 to study changes in central and peripheral monitoring signals during controlled hypovolemia, which is a condition of decreased blood volume. The study aims to find the best site on the body to monitor hypovolemia using pulse oximeter waveforms from various locations including the finger, ear, forehead, and nose. It also evaluates other measurements such as blood pressure, cerebral oximetry, and peripheral venous pressure during gradual blood volume reduction. Participants will undergo gradual hypovolemia induced by lower body negative pressure (LBNP), a method that simulates blood loss by applying suction to the lower body. During this process, continuous monitoring of pulse oximeter waveforms and other hemodynamic parameters will be conducted to observe changes. The study collects data to identify which peripheral site provides the most reliable monitoring for hypovolemia. Volunteers will be monitored closely throughout the procedure with various devices tracking cardiovascular and respiratory signals. The primary outcome is determining the most robust monitoring site for hypovolemia using pulse oximetry over a period of two years. Secondary measures include examining the connection between central heart function and respiratory changes seen in pulse oximeter signals during hypovolemia and fluid resuscitation. The total participation duration and follow-up are aligned with these measurement periods.
CONDITIONS
Brief Title
Hemodynamics Monitoring During Lower Body Negative Pressure (LBNP) Induced Controlled Hypovolemia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy volunteers aged 20 to 45 years
You will not qualify if you...
- Pregnant women
- Under 20 years of age
- Subjects with coronary artery disease, diabetes, epilepsy, and hypertension
AI-Screening
AI-Powered Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 day
Participants undergo monitoring of hemodynamic changes during lower body negative pressure induced controlled hypovolemia.
1 visit (in-person)
Duration - 2 years
Participants are observed for changes in pulse oximeter waveforms and central hemodynamics over a 2-year period.
Trial Site Locations
Total: 1 location
1
John B. Pierce Laboratory
New Haven, Connecticut, United States, 06520
Actively Recruiting
Research Team
A
Aymen Alian, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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