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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03179033
Other study ID # SHEBA-16-3259-ER-CTIL
Secondary ID
Status Completed
Phase N/A
First received June 5, 2017
Last updated January 17, 2018
Start date October 19, 2016
Est. completion date August 30, 2017

Study information

Verified date June 2017
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date August 30, 2017
Est. primary completion date August 30, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients after VAD implantation

Exclusion Criteria:

- Age under 18

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Sheba medical center Ramat Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Responsiveness to passive leg raising in patients early after LVAD implantation Change in LVAD flow due to passive leg raising 5 minutes
See also
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Recruiting NCT06102226 - Deep Learning Algorithm for Detecting Obstructive Coronary Artery Disease Using Fundus Photographs
Active, not recruiting NCT01981642 - Noninvasive Diagnostics in Left Ventricular Assist Device Patients N/A