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AI may help anesthesiologists avoid airway emergencies in obese patients

NCT ID NCT07666074

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether artificial intelligence can better predict difficult airway management in 340 obese patients undergoing bariatric surgery. Researchers will compare AI predictions using standard measurements like mouth opening and neck length against actual views during intubation. If accurate, AI could help doctors prepare safer anesthesia plans.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Artificial intelligence algorithm
What this could lead to
If successful, this could lead to a more accurate tool for predicting difficult airways, potentially reducing complications during anesthesia in obese patients.
What could go wrong
This is an early-stage study with 340 participants, so results may not apply to all patients. AI predictions may not outperform traditional methods, and the study does not test a treatment.

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.

Participants

About 340 people

The number the study aims to enrol. It can still change while the study runs.

Started

May 2026

Expected to finish

Oct 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.

Who is studied

The study population consists of adult obese patients (BMI ≥ 35 kg/m²) undergoing elective bariatric surgery under general anesthesia in a tertiary academic medical center. This population represents individuals at a higher baseline risk for difficult airway management and intubation.

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: 1. Adult patients aged 18 to 65 years. 2. Scheduled for elective bariatric surgery under general anesthesia. 3. Body Mass Index (BMI) ≥ 35 kg/m². 4. Consenting to participate in the study. Exclusion Criteria: 1. Patients with known upper airway anatomical deformities, head and neck tumors, or a history of head/neck radiotherapy. 2. History of maxillofacial, airway, or cervical spine surgery. 3. Emergency surgeries. 4. Patients requiring planned awake fiberoptic intubation based on obvious preoperative clinical indicators.

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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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Fethi Sekin City Hospital

    RECRUITING

    Elâzığ, Elâzığ, 23100, Turkey (Türkiye)

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