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Change in Stroke Volume Index After Diuresis for Patients With Decompensated Heart Failure

Change in Stroke Volume Index After Diuresis for Patients With Decompensated Heart Failure

Status
Suspended
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05240651
Enrollment
50
Registered
2022-02-15
Start date
2022-08-30
Completion date
2027-07-01
Last updated
2026-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Decompensated Heart Failure

Brief summary

This is a prospective cohort study for 50 patients admitted to the cardiac care unit requiring clinically-indicated diuretic therapy for congestive heart failure. The purpose of this study is to assess the role of non-invasive cardiac output monitoring (NICOM) with the Starling Fluid Management System (Baxter Medical, Deerfield, IL) in determining volume status in patients with acute decompensated heart failure requiring intravenous diuretic therapy.

Interventions

None listed

Sponsors

NYU Langone Health
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Diagnosis of congestive acute decompensated heart failure (preserved or reduced ejection fraction) requiring clinically indicated IV diuresis 2. Admission to coronary/cardiac intensive care unit or cardiac step down unit 3. Able to provide written informed consent 4. Anticipated need for IV diuretics \> 24 hrs

Exclusion criteria

1. Prisoner, pregnancy or post-partum stage, or age \< 18 years 2. Known allergy to sensory material or gel 3. End stage renal disease or need for CRRT 4. Inability or contraindication to do a passive leg raise with both extremities (i.e., balloon pump, impella, spinal injury, amputation) 5. Other situation that might increase subject risk, interfere with study procedures, or confound study findings based on the opinion of the clinician/investigator 6. Inability to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Percent Change in Stroke Volume Index (SVI) after passive leg raise (PLR)Baseline, At Discharge (up to 1 week)The Startling System non-invasive cardiac output monitoring (NICOM) device will use a proprietary algorithm to determine SVI. A passive leg raise (PLR) is then performed to increase preload and then the Starling System takes a second set of measurements to determine the parameters above as well as the change in stroke volume index.

Secondary

MeasureTime frameDescription
Change in Stroke Volume Index (SVI) before passive leg raise (PLR)Baseline, At Discharge (up to 1 week)The Startling System non-invasive cardiac output monitoring (NICOM) device will use a proprietary algorithm to determine SVI. A passive leg raise (PLR) is then performed to increase preload and then the Starling System takes a second set of measurements to determine the parameters above as well as the change in stroke volume index.
Change in Stroke Volume Index (SVI) after passive leg raise (PLR)Baseline, At Discharge (up to 1 week)The Startling System non-invasive cardiac output monitoring (NICOM) device will use a proprietary algorithm to determine SVI. A passive leg raise (PLR) is then performed to increase preload and then the Starling System takes a second set of measurements to determine the parameters above as well as the change in stroke volume index.
Change in estimated Cardiac Output (CO) before passive leg raise (PLR)Baseline, At Discharge (up to 1 week)The Startling System non-invasive cardiac output monitoring (NICOM) device will use a proprietary algorithm to determine CO. A passive leg raise (PLR) is then performed to increase preload and then the Starling System takes a second set of measurements to determine the parameters above as well as the change in CO.
Change in estimated Cardiac Output (CO) after passive leg raise (PLR)Baseline, At Discharge (up to 1 week)The Startling System non-invasive cardiac output monitoring (NICOM) device will use a proprietary algorithm to determine CO. A passive leg raise (PLR) is then performed to increase preload and then the Starling System takes a second set of measurements to determine the parameters above as well as the change in CO.
Change in estimated Cardiac Index (CI) before passive leg raise (PLR)Baseline, At Discharge (up to 1 week)The Startling System non-invasive cardiac output monitoring (NICOM) device will use a proprietary algorithm to determine CI. A passive leg raise (PLR) is then performed to increase preload and then the Starling System takes a second set of measurements to determine the parameters above as well as the change in CI.
Change in estimated Cardiac Index (CI) after passive leg raise (PLR)Baseline, At Discharge (up to 1 week)The Startling System non-invasive cardiac output monitoring (NICOM) device will use a proprietary algorithm to determine CI. A passive leg raise (PLR) is then performed to increase preload and then the Starling System takes a second set of measurements to determine the parameters above as well as the change in CI.
Change in heart rate before passive leg raise (PLR)Baseline, At Discharge (up to 1 week)
Change in heart rate after passive leg raise (PLR)Baseline, At Discharge (up to 1 week)
Change in Mean arterial pressure before passive leg raise (PLR)Baseline, At Discharge (up to 1 week)
Change in Mean arterial pressure after passive leg raise (PLR)Baseline, At Discharge (up to 1 week)

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORCarlos Alviar, MD

NYU Langone Health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026