New airway device shows promise for obese surgery patients
NCT ID NCT07573813
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a new video laryngeal mask airway (SaCoVLM™) in 57 morbidly obese patients undergoing bariatric surgery. The device helped doctors place a breathing tube on the first try in most cases. The goal was to see if it is safe and effective for this group of patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- SaCoVLM™ video laryngeal mask airway (device)
- What this could lead to
- If successful, this device could make intubation safer and easier for obese patients undergoing surgery.
- What could go wrong
- This is a small, single-arm study with no comparison group, so results may not apply to all patients. The device is still new and needs more testing.
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
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57 people
The number who actually took part.
- Started
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May 2022
- Finished
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May 2023
- 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
The study population comprised adult patients aged over 18 years (with no upper age limit) diagnosed with morbid obesity.
- 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: 1. Adult patients aged over 18 years (no upper age limit) 2. Diagnosed with morbid obesity, clinically defined as either: Body mass index (BMI) ≥ 40 kg/m², or BMI ≥ 35 kg/m² accompanied by at least one significant obesity-related comorbidity Exclusion Criteria: 1. Have no clinical indicators of anticipated difficult airway (Mallampati classification IV, thyromental distance \< 6 cm, mouth opening \< 3 cm, severe limited neck extension, or a history of difficult airway management) 2. Demonstrate tolerance for laparoscopic surgery and anesthesia 3. Be scheduled exclusively for LSG without concurrent additional procedures
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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.
Contacts and locations
Locations
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The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital
Jinan, Shandong, 250014, China
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Other studies related to the condition(s) this trial covers.
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