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Comparison of Subcostal and Transhepatic Views to Assess Inferior Vena Cava by Echocardiography (VCI ECHO)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03587090
Recruitment Status : Completed
First Posted : July 16, 2018
Last Update Posted : January 22, 2020
Sponsor:
Information provided by (Responsible Party):
University Hospital, Caen

Study Description
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Brief Summary:
Comparison of subcostal and transhepatic views to measure inferior vena cava diameter by echocardiography in intensive care unit patients

Condition or disease Intervention/treatment
Inferior Vena Cava Diameter Diagnostic Test: echocardiography

Study Design
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Study Type : Observational
Actual Enrollment : 131 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Comparaison échographique Des Voies Sous Costale et Trans hépatique Dans l'évaluation de la Veine Cave inférieure
Actual Study Start Date : May 14, 2018
Actual Primary Completion Date : October 4, 2019
Actual Study Completion Date : October 4, 2019
Groups and Cohorts
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Intervention Details:
  • Diagnostic Test: echocardiography
    echocardiography by subcostal and transhepatic views

Outcome Measures
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Primary Outcome Measures :
  1. inferior vena cava diameter [ Time Frame: up to 1 day after inclusion ]
    measurement of inferior vena cava diameter by 2D et TM mode


Eligibility Criteria
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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
intensive care unit patients
Criteria

Inclusion Criteria:

  • patient hospitalised in ICU

Exclusion Criteria:

  • gardianship
  • contraindication to transthoracic echocardiography
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03587090


Locations
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France
Service de réanimation médicale CHU de Caen
Caen, France, 14033
Sponsors and Collaborators
University Hospital, Caen
More Information
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Responsible Party: University Hospital, Caen
ClinicalTrials.gov Identifier: NCT03587090    
Other Study ID Numbers: caenUH 18-034
First Posted: July 16, 2018    Key Record Dates
Last Update Posted: January 22, 2020
Last Verified: June 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No