Diaphragm Response in Elderly for Acute Monitoring

NCT ID: NCT07132268

Last Updated: 2026-01-05

Study Results

Results pending

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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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

145 participants

Study Classification

OBSERVATIONAL

Study Start Date

2026-01-31

Study Completion Date

2028-01-31

Brief Summary

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Acute dyspnea is a common cause of emergency department admissions among elderly patients. Acute respiratory failure is often multifactorial and requires rapid and reliable evaluation. Currently, management relies on clinical, biological, and radiological assessments, but diaphragmatic ultrasound could provide an additional tool for real-time respiratory function evaluation. This study aims to integrate this non-invasive technology into the initial assessment of patients to improve care pathways. Hypothesis : Diaphragmatic ultrasound enables reliable assessment of respiratory function and can predict the need for mechanical ventilation.

Detailed Description

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Conditions

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Acute Dyspnea Acute Respiratory Failure Diaphragmatic Ultrasound

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Patients aged ≥ 75 years
* Emergency admission for acute dyspnea
* Requiring an emergency ultrsoung.

Exclusion Criteria

* Acute respiratory distress requiring immediate invasive or non-invasive ventilation
* 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
Minimum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier de Bethune

NETWORK

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Centre Hospitalier de Béthune

Béthune, , France

Site Status

Centre Hospitalier de Douai

Douai, , France

Site Status

Centre Hospitalier Emile Roux

Le Puy-en-Velay, , France

Site Status

Centre Hospitalier Sud Ile-de-France

Melun, , France

Site Status

Centre Hospitalier de Roubaix

Roubaix, , France

Site Status

Centre Hospitalier de Saint-Lô

Saint-Lô, , France

Site Status

Centre Hospitalier de Tourcoing

Tourcoing, , France

Site Status

Centre Hospitalier de Valenciennes

Valenciennes, , France

Site Status

Countries

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France

Central Contacts

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Tristan CARRIE, Doctor

Role: CONTACT

03.21.64.70.84

Facility Contacts

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Mélanie VERLAY

Role: primary

0602013068

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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