Actively Recruiting
Sonographic Diaphragm Function in AECOPD
Led by Isala · Updated on 2024-10-04
51
Participants Needed
1
Research Sites
122 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Sonographic Diaphragm Function in AECOPD
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Hospitalisation primarily because of severe acute exacerbation of COPD
- COPD diagnosed according to GOLD 2018 definition
- Post-bronchodilator FEV1/FVC < 0.70 and FEV1% < 80% predicted within the last 5 years
You will not qualify if you...
- Respiratory acidosis (pH < 7.35 and PaCO2 > 6 kPA)
- Need for (non-)invasive ventilation due to other criteria such as severe hypoxia at presentation
- Established diagnosis of diaphragm paralysis
- Inability to undergo diaphragm imaging (e.g., mechanical ventilation or unable to follow vocal instructions)
- Unable or unwilling to give written informed consent
- Pregnant women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Isala Klinieken
Zwolle, Overijssel, Netherlands, 8025AB
Actively Recruiting
Research Team
W
wytze s de Boer, m.d.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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