Prevalence and Kinetics of Diaphragmatic Dysfunction in Elderly Patients With Acute Respiratory Distress
NCT ID: NCT04520815
Last Updated: 2021-10-06
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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UNKNOWN
100 participants
OBSERVATIONAL
2020-06-24
2022-06-30
Brief Summary
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To our knowledge, there is no data available in the literature on the prevalence of diaphragmatic dysfunction and its short- and long-term course in this category of patients. The main objective of this study is therefore to assess the prevalence of diaphragmatic dysfunction and its evolutionary kinetics in patients over the age of 75 admitted for acute respiratory distress in the emergency medicine department.
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Detailed Description
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Conditions
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Study Design
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COHORT
OTHER
Eligibility Criteria
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Inclusion Criteria
* Presence of acute respiratory distress defined by at least 1 of the following criteria:
* Respiratory rate \> 25/min and/or clinical signs of acute respiratory distress,
* Hypoxia defined by Sp02 \< 90 %,
* Hypercapnia defined by PaC02 \> 45 mmHg with respiratory acidosis defined by a pH value \<7.35.
* Absence of opposition of the patient to his participation in the study and the use of his data or the trusted person if the state of the patient does not allow it.
Exclusion Criteria
* Patient with acute respiratory distress on arrival at the SAU with clinical criteria justifying immediate use of invasive mechanical ventilation and not allowing ultrasound measurements to be carried out or patient admitted to the SAU with mechanical ventilatory support from the outset,
* Poor command of the French language or state incompatible with the patient's understanding and / or informed adherence to the study protocol,
* History of surgery involving the integrity of the diaphragmatic muscle (diaphragm plication or diaphragmatic lumpectomy or placement of diaphragmatic pacemaker),
* Criteria for shock or severe hemodynamic instability,
* Intra-cranial hypertension.
75 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de la Réunion
OTHER
Responsible Party
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Principal Investigators
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Thomas GROSEIL, Dr
Role: PRINCIPAL_INVESTIGATOR
CHU de La Réunion
Locations
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Centre Hospitalier Universitaire de la Réunion
Saint-Denis, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2020/CHU/10
Identifier Type: -
Identifier Source: org_study_id
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