New belt could help obese patients breathe easier during surgery
NCT ID NCT06518239
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a special belt that uses electrical currents to measure lung function in 30 obese patients during laparoscopic surgery. The goal was to see if the belt could set the breathing machine pressure better than standard methods. The results may help improve breathing support and reduce complications for obese patients undergoing surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- EIT belt (electrical impedance tomography device)
- What this could lead to
- If successful, this could lead to better breathing support during surgery for obese patients, reducing complications.
- What could go wrong
- This is a small pilot study with only 30 participants, so results may not apply broadly. The device is experimental and may not outperform standard care.
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
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30 people
The number who actually took part.
- Started
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Nov 2024
- Finished
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Mar 2026
- 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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19 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. BMI ≥ 40 kg/m2 2. Age \> 18 years 3. Scheduled for elective laparoscopic abdominal surgery in the steep Trendelenburg position. 4. Able to provide informed consent. Exclusion Criteria: 1. Currently pregnant. 2. Presence of pacemaker, neurostimulator, spinal cord stimulator, or implantable cardioverter-defibrillator. 3. Skin ulcerations on upper torso near the belt placement. 4. Presence of phrenic nerve palsy or other diaphragm conditions. 5. Thoracic circumference \> 134 cm. 6. Tracheomalacia. 7. Inability to speak and understand English.
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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
-
University Hospital
Columbia, Missouri, 65212, United States
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