Ultrasound could replace breathing tests for diaphragm strength
NCT ID NCT04959526
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares a new ultrasound technique (shear-wave elastography) to standard breathing tests for measuring diaphragm muscle forces. Researchers will test 24 healthy adults during various breathing maneuvers and nerve stimulation. The goal is to see if the ultrasound method can reliably measure diaphragm strength, potentially offering a simpler, non-invasive alternative for future clinical use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a simpler, non-invasive way to assess diaphragm function using ultrasound.
- What could go wrong
- This is a small, early study in healthy volunteers only. It may not translate to patients with lung disease, and the ultrasound method may not match current testing accuracy.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 24 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jul 2021
- Expected to finish
-
Dec 2026
An estimate. End dates often move.
- Lead sponsor
-
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.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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: \- Adult male and female healthy volunteers. Exclusion Criteria: * Volunteers who are pregnant. * Volunteers with known pulmonary pathology (COPD, asthma requiring routine treatment).
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Respiratory complication are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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.
Contacts and locations
Locations
-
Mayo Clinic in Rochester
RECRUITINGRochester, Minnesota, 55905, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A smarter mask may spot breathing trouble before it starts
- Smart mask alarms may spot breathing trouble before it turns critical
- Which nerve block keeps lungs stronger after chest surgery?
- Can 3D motion capture reveal hidden breathing problems after esophageal cancer surgery?
- Heartbeat clues may flag surgery risks in children
- Does a stomach tube prevent breathing problems in babies with pyloric stenosis?