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Usefulness of an Ultraportative Ultrasound Device in the Management of Intra Hospital Emergencies

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ClinicalTrials.gov Identifier: NCT02967809
Recruitment Status : Completed
First Posted : November 18, 2016
Last Update Posted : April 27, 2020
Sponsor:
Information provided by (Responsible Party):
Hospital Nord

Brief Summary:

Estimate if the use of a portable cardiac echograph for intra-hospital Emergencie improves the performances diagnose in the bed of patient in department of conventional medicine.

The concordance between the initial medical diagnosis (previous the utilsation of portable echograph) and the final diagnosis (after portable echograph utisation) will be evaluated. These evaluation will be performed after retrospective review of the medical files


Condition or disease Intervention/treatment
Respiratory Failure Failure; Cardiac Device: echography

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Study Type : Observational [Patient Registry]
Actual Enrollment : 172 participants
Observational Model: Case-Control
Time Perspective: Prospective
Target Follow-Up Duration: 1 Month
Official Title: Usefulness of an Ultraportative Ultrasound Device in the Management of Intra Hospital Emergencies
Actual Study Start Date : October 2016
Actual Primary Completion Date : November 2018
Actual Study Completion Date : September 2019

Resource links provided by the National Library of Medicine


Group/Cohort Intervention/treatment
final diagnosis after portable echography
Experimental group: final diagnosis after portable cardiac echograph examination
Device: echography
cardiac and pulmonary echography

final diagnosis without portable echography
Group control: Final diagnosis for patient ( same medical condition and history) hospitalized in units without portable cardiac echograph examination avaible



Primary Outcome Measures :
  1. Concordance between initial medecial diagnosis and final diagnosis [ Time Frame: 1 day ]
    Concordance between the initial medical diagnosis at the bedside in ward and the definitive diagnosis after retrospective review of the medical files between two groups : one with an ultraportative echograph (POCUS group) and a control (without ultraportative group). The percentage of adequate initiale diagnosis at the bedside.



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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
Patient suffering of respiratory or cardiac distress
Criteria

Inclusion Criteria:

  • respiratory or cardiac distress

Exclusion Criteria:

  • pulmonary or cardiac patient transplant morphologic abnormalities Patient in rescucitation care unit

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): NCT02967809


Locations
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France
Departement anesthesie reanimation hopital nord
Marseille, France, 13015
Sponsors and Collaborators
Hospital Nord
Investigators
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Principal Investigator: Marc Leone, MD DAR Nord
Additional Information:

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Hospital Nord
ClinicalTrials.gov Identifier: NCT02967809    
Other Study ID Numbers: 00010254 --- 2016 --- 122
First Posted: November 18, 2016    Key Record Dates
Last Update Posted: April 27, 2020
Last Verified: April 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Additional relevant MeSH terms:
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Respiratory Insufficiency
Emergencies
Disease Attributes
Pathologic Processes
Respiration Disorders
Respiratory Tract Diseases