Monitoring blood flow changes during controlled low blood volume conditions
Official title: Hemodynamics Monitoring During Lower Body Negative Pressure (LBNP) Induced Controlled Hypovolemia
Run by Yale University · NCT03592290 · Data updated 2026-11-12
This study is testing how lowering blood volume affects blood flow in healthy people to find the best ways to monitor these changes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 20 Years to 45 Years |
| Sex | All |
| Enrollment | 120 (estimated) |
| Sponsor | Yale University Academic / other |
| Locations | 1 site (New Haven, Connecticut) |
| Status | Recruiting |
| Started | November 15, 2017 |
| Main results expected | January 2027 |
| Study ends | January 2027 |
| Registry record updated | January 20, 2026 |
| Trial ID | NCT03592290 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are healthy volunteers aged 20-45 without any underlying health conditions.
✕Probably not a fit
Patients with coronary artery disease, diabetes, epilepsy, hypertension, or those who are pregnant will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This research aims to monitor the effects of lower body negative pressure (LBNP) on hemodynamics by inducing controlled hypovolemia in healthy volunteers. The study will assess changes in central and peripheral waveforms, including those from pulse oximeters placed on various body sites such as the finger, ear, forehead, and nose. Additionally, blood pressure, cerebral oximetry, and peripheral venous pressure will be measured to identify the most effective monitoring sites for hypovolemia. The findings could enhance our understanding of hemodynamic instability and improve monitoring techniques.
Why it matters
Potential benefit: If successful, this study could lead to improved methods for monitoring blood volume changes, which is crucial for managing patients with hemodynamic instability.
How similar studies have gone: While this approach is observational and may not have been extensively tested in this specific context, similar studies have shown promise in monitoring hemodynamic changes.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: \* Healthy volunteers aged 20-45 with Exclusion Criteria: * Pregnant women * Under 20 years of age * Subjects with coronary artery disease, diabetes, epilepsy and hypertension
Where it's running
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John B. Pierce Laboratory
New Haven, Connecticut, United States Recruiting
Study contacts
- Principal investigator: Aymen Alian, MD — Yale University
- Study coordinator: Aymen Alian, MD
- Email: aymen.alian@yale.edu
- Phone: 203-785-2802
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.