CourbePVC: Continuous Monitoring of Right Ventricular Function, Based on the Correlation Between the C-X Segment of the Central Venous Pressure Curve, and the Echocardiographic Evaluation of Right Ventricular Systolic Function

Sponsor
Centre Hospitalier Universitaire Dijon (Other)
Overall Status
Unknown status
CT.gov ID
NCT03295669
Collaborator
(none)
250
1
12
20.8

Study Details

Study Description

Brief Summary

Close analysis of right ventricular function is still not done by all clinicians, even though it is indispensable; notably in cardiovascular ICUs.

Right ventricular dysfunction is responsible for increased morbidity and marks a turning point in the patient's prognosis.

It is difficult to analyse, and is principally assessed using echocardiography and by measuring the peak of the S' wave with pulsed Doppler and by measuring the tricuspid annular plane systolic excursion (TAPSE) in the TM mode. New studies have shown the interest of using 2D strain as a marker of systolic and diastolic function of the right ventricle. Finally, the use of 3D ultrasound seems to be more reliable than cardiac MRI for fine analysis of the right ventricle, even though it is rarely used in routine practice.

Study of the right ventricle using ultrasonography alone requires experienced and available operators for closely repeated evaluations making it possible to detect right ventricle dysfunction quickly.

US monitoring of left and right heart function is done systematically and repeatedly during post-operative care following heart surgery. This US evaluation could be optimized by finding a way to monitor the right ventricle continuously.

From a physiological point of view, we know about the tight relationship between the aspect of the central venous pressure curve and more precisely the C-X segment (tricuspid bulging into the atrium and start of contraction of the right ventricle) and right ventricular function. We wish to analyse this segment, combined with a US evaluation, and to look for a possible correlation so as to allow continuous, easy-to-interpret monitoring of right ventricular systolic function.

This will be facilitated by the systematic presence of a central venous catheter in every patient undergoing heart surgery, thus allowing central venous pressure to be monitored.

To this end, we wish to collect different data from patients in the cardiovascular ICU, especially the central venous pressure curve, the ventilatory pressure curve and settings of the respirator, and to carry out an echography evaluation of each patient.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    250 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Continuous Monitoring of Right Ventricular Function, Based on the Correlation Between the C-X Segment of the Central Venous Pressure Curve, and the Echocardiographic Evaluation of Right Ventricular Systolic Function
    Study Start Date :
    Nov 1, 2016
    Anticipated Primary Completion Date :
    Nov 1, 2017
    Anticipated Study Completion Date :
    Nov 1, 2017

    Outcome Measures

    Primary Outcome Measures

    1. Measure the peak of the S' wave [At baseline]

    2. Measure the tricuspid annular plane systolic excursion (TAPSE) [At baseline]

    3. Calculate strain in the right ventricle [At baseline]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients admitted to the cardiovascular ICU

    • Patients with spontaneous breathing

    • With a central venous catheter placed in the internal jugular vein and for whom the central venous pressure curve is exploitable

    • With a US window allowing a 4-chamber view making it possible to calculate the right ventricle ejection fraction (Peak of the S' wave, of the TAPSE, Strain of the right ventricle)

    Exclusion Criteria:
    • Non-echogenic patients or those without an exploitable US window

    • Patients without a central venous catheter in the internal jugular vein

    • Patients with an unexploitable central venous pressure curve

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Chu Dijon Bourogne Dijon France

    Sponsors and Collaborators

    • Centre Hospitalier Universitaire Dijon

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Centre Hospitalier Universitaire Dijon
    ClinicalTrials.gov Identifier:
    NCT03295669
    Other Study ID Numbers:
    • ELLOUZE 2016
    First Posted:
    Sep 28, 2017
    Last Update Posted:
    Sep 28, 2017
    Last Verified:
    Sep 1, 2017
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 28, 2017