Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
89700 participants
OBSERVATIONAL
2024-09-30
2031-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patients with acute dyspnea managed by a medical emergency team at the investigator centers between 2010 and 2021.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Pr. Nicolas GIRERD
OTHER
Responsible Party
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Pr. Nicolas GIRERD
Clinical Professor
Principal Investigators
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Tahar CHOUIHED, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Central Hospital, Nancy, France
Nicolas GIRERD, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
CHRU de Nancy
Locations
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CHU de Besançon
Besançon, , France
CHU de Dijon
Dijon, , France
Hospices civils de Lyon, Groupement Hospitalier Édouard-Herriot
Lyon, , France
CHRU of Nancy
Nancy, , France
Countries
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Central Contacts
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Facility Contacts
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Omide TAHERI
Role: primary
Patrick RAY, MD, PhD
Role: primary
Stephanie BOSNE, MD
Role: primary
Other Identifiers
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2022PI21
Identifier Type: -
Identifier Source: org_study_id
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