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
145 participants
OBSERVATIONAL
2026-01-31
2028-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Emergency admission for acute dyspnea
* Requiring an emergency ultrsoung.
Exclusion Criteria
* Respiratory rate ≥ 25 breaths/min, and/or SpO2 ≤ 90% on room air, and/or PaO2 ≤ 60 mmHg
* Known diaphragmatic paralysis
* Patients with degenerative neuromuscular disease
* State of shock: systolic blood pressure \< 90 mmHg and/or mean arterial pressure \< 65 mmHg and/or presence of skin mottling and/or CTR \> 3s
* Lactate levels \> 2 mmol/L
* Hypercapnic respiratory acidosis (pH \< 7.38 and PaCO2 \> 45 mmHg)
* Dyspnea due to metabolic acidosis (e.g., diabetic ketoacidosis, renal failure)
* Dyspnea of traumatic origin
* Refusal to participate or inability to provide informed consent
* Patients deprived of liberty
* Patients under guardianship or curatorship
75 Years
ALL
No
Sponsors
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Centre Hospitalier de Bethune
NETWORK
Responsible Party
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Principal Investigators
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Alain-Eric DUBART
Role: STUDY_DIRECTOR
Centre Hospitalier de Béthune-Beuvry
Locations
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Centre Hospitalier Victor Dupouy
Argenteuil, , France
Centre Hospitalier de Béthune
Béthune, , France
Centre Hospitalier de Douai
Douai, , France
Centre Hospitalier Emile Roux
Le Puy-en-Velay, , France
Centre Hospitalier Sud Ile-de-France
Melun, , France
Centre Hospitalier de Roubaix
Roubaix, , France
Centre Hospitalier de Saint-Lô
Saint-Lô, , France
Centre Hospitalier de Tourcoing
Tourcoing, , France
Centre Hospitalier de Valenciennes
Valenciennes, , France
Countries
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Central Contacts
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Facility Contacts
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Role: backup
Other Identifiers
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ID-RCB
Identifier Type: OTHER
Identifier Source: secondary_id
2025-01
Identifier Type: -
Identifier Source: org_study_id
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