New study aims to perfect diaphragm measurement in ICU patients
NCT ID NCT07559669
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study involves 35 critically ill adults to see if different ultrasound methods give consistent measurements of left diaphragm movement. Researchers will compare standard and modified positions to find the most reliable technique. The goal is to improve how doctors assess diaphragm function in intensive care.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 35 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Critically ill patients
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * ①Adult patients (≥18 years old) of both sexes; * In invasive group, intubation or tracheotomy was changed to 5L/min T-tube or tracheotomy mask oxygen inhalation; * Patients in non-invasive group were treated with mask oxygen 5L/min; * agree to participate in the trial and sign the informed consent; Exclusion Criteria: * ①The diaphragm ultrasound operation site was too large to obtain images. * Diaphragmatic ultrasound images could not be obtained in any section; * The ultrasound image quality of any section was poor; * the presence of phrenic nerve injury/paralysis ⑤ pregnant women; ⑥ Neuromuscular diseases such as ALS and myasthenia gravis affect the evaluation of spontaneous breathing ⑦ Patients deemed by the investigator to be ineligible.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.
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