Ultrasound may make intubation safer for obese patients
NCT ID NCT07482436
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether using ultrasound before and after surgery can help predict difficult breathing tube placement in obese patients. It will compare standard checks with ultrasound measurements and test different types of laryngoscopes. The goal is to improve safety and reduce complications during intubation.
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 safer intubation methods for obese patients by using ultrasound to predict difficulties.
- What could go wrong
- This is an early-stage observational study, not a treatment trial. Results may not apply to all patients or settings.
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
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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
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About 180 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Jul 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.
- 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: * Patients who have given their consent * Patients who underwent surgery under general anesthesia * Patients over eighteen years of age * Patients with an American Society of Anesthesiologists (ASA) physical status classification of I-II-III * Patients with a body mass index (BMI) of 30 kg/m2 or higher * Patients whose surgery lasts between 60 and 150 minutes * Patients who underwent surgery under elective conditions will be included. Exclusion Criteria: * Patients who do not consent, * those undergoing head and neck surgery, * those to be operated on in the prone position, * uncooperative patients (patients with whom communication is not possible), * those with craniofacial anomalies, * patients operated on in emergency situations will be excluded from the study.
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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 places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
Contacts and locations
Locations
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Trabzon University Faculty of Medicine Kanuni Training and Research Hospital
RECRUITINGTrabzon, 61040, Turkey (Türkiye)
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