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NCT03179033

Impact of Fluid and Passive Leg Raising on Cardiac Output in Patients Undergoing Cardiac Surgery

Completed Last updated 18 January 2018
What this trial tests

trial in Artificial Heart Device User in 20 participants. Completed in 30 August 2017.

Timeline
19 October 2016
Primary endpoint
30 August 2017
30 August 2017

Quick facts

Lead sponsorSheba Medical Center
StatusCompleted
Study typeOBSERVATIONAL
Enrollment20
Start date19 October 2016
Primary completion30 August 2017
Estimated completion30 August 2017
Sites1 location across Israel

Conditions studied

Sponsor

Sheba Medical Center

Who can join

18 and older, any sex, with Artificial Heart Device User. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Left Ventricular Assist Device (LVAD) implantation is a common surgical procedure in patients with end-stage heart failure. Optimal fluid management is essential for adequate postoperative treatment. It is important to identify which patients will benefit from fluid administration. Passive leg raising (PLR) is a validated dynamic method to predict fluid responsiveness in patients with heart failure by inducing a transient increase in cardiac preload. Objective: To investigate the role of PLR on the management of patients following LVAD implantation in the postoperative period.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Sheba Medical Center trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03179033.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing