- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02967809
Usefulness of an Ultraportative Ultrasound Device in the Management of Intra Hospital Emergencies
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
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Marseille, France, 13015
- Departement anesthesie reanimation hopital nord
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- respiratory or cardiac distress
Exclusion Criteria:
- pulmonary or cardiac patient transplant morphologic abnormalities Patient in rescucitation care unit
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
final diagnosis after portable echography
Experimental group: final diagnosis after portable cardiac echograph examination
|
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
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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.
|
1 day
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Marc Leone, MD, DAR Nord
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 00010254 --- 2016 --- 122
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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