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Sonographic Diaphragm Function in AECOPD — UNDATED  

Copd Clinical Trial

Official title:
Ultrasound of the Diaphragm as Physiological Biomarker in Acute Exacerbations of Chronic Obstructive Pulmonary Disease

Clinical Trial Summary

The study will be conducted as a single-center, prospective cohort study. The primary objective of this study is to investigate the responsiveness of sonographic parameters of diaphragm to detect change in Borg score for dyspnea during hospitalisation for AECOPD without respiratory acidosis.

Clinical Trial Description

To investigate the responsiveness of sonographic parameters to detect change in Borg score for dyspnea during hospitalisation for AECOPD without respiratory acidosis, we propose a prospective cohort design. After inclusion, participants will have assessment of diaphragm function (excursion, thickness, thickening fraction) using ultrasound within 48 hours of admission to the emergency ward, striving to assessment within 24 hours of admission. Additionally, dyspnea grade will be assessed using validated questionnaires. Further diagnostic work-up and treatment for AECOPD is performed at the discretion of the treating physician. Both ultrasound measurements and dyspnea grade questionnaires will be repeated when the participant is reported suitable for hospital discharge by the treating physician. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05671198
Study type Observational
Source Isala
Contact
Status Recruiting
Phase
Start date March 27, 2023
Completion date August 2024
View Details
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