Actively Recruiting

Age: 20Years - 45Years
All Genders
Healthy Volunteers
ID03592290

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

Age: 20Years - 45Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy volunteers aged 20 to 45 years
Not Eligible

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

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - 1 day

Participants undergo monitoring of hemodynamic changes during lower body negative pressure induced controlled hypovolemia.

1 visit (in-person)

Long-term Monitoring

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

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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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