New oxygen technique aims to prevent low oxygen during uterine surgery
NCT ID NCT07110428
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a special oxygen delivery method (supraglottic jet ventilation) can prevent low oxygen levels during hysteroscopic surgery. 100 women will be randomly assigned to receive either standard oxygen via a nasal cannula or the new jet ventilation. The main goal is to see if the new method reduces episodes of dangerously low oxygen.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- supraglottic jet oxygen ventilation (SJOV) via a nasal tube
- What this could lead to
- If it works, this could offer a safer way to keep oxygen levels stable during hysteroscopic surgery, reducing complications like low oxygen and sore throat.
- What could go wrong
- This is a small, early-stage study (100 patients) comparing two oxygen methods. Results may not apply to all patients or surgeries, and the technique may not reduce risks as hoped.
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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Mar 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 to 65 years
- Sex
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Female participants only
- 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: * Age between 18 and 65 years, with American Society of Anesthesiologists (ASA) I-II; * Body mass index (BMI) between 18 and 28 kg/m²; * Scheduled for elective hysteroscopic surgery under anesthesia * Signed written informed consent exclusion criteria: * Any upper airway abnormalities that may cause difficult airway management, such as limited mouth opening, Mallampati Class ≥ III, and abnormal neck mobility; history of respiratory insufficiency or sleep apnea, with STOP-BANG score \>3; * Chronic alcohol abuse or drug abuse ; * Current use of anticoagulant medications; * Nasal, oropharyngeal infections or other contraindications for nasopharyngeal airway/WNJ insertion, including active rhinitis, recent nasal surgery, epistaxis, nasal polyps, or nasal stenosis; * Allergy to study medications ; * Intraoperative conversion to endotracheal intubation due to expanded surgical scope or participant's withdrawal of consent.
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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Peking University Shenzhen Hospital
Guangdong, Shenzhen, 518000, China