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New Tube-Guiding technique may speed up stomach surgery prep

NCT ID NCT06730984

Knowledge-focused Sponsor: Ningbo No. 1 Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether using a small camera (endoscope) to guide the breathing tube into the windpipe is faster and less uncomfortable than the usual method with a video laryngoscope. It involved 132 adults having a procedure called endoscopic submucosal dissection (ESD) to remove early-stage stomach growths. Researchers measured how long preparation took and how patients felt afterward.

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 show that using an endoscope to guide breathing tube placement is faster and more comfortable for patients having ESD.
What could go wrong
This is a small, single-center study focused on timing and comfort, not on curing or treating a disease. Results may not apply to other procedures or hospitals.

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

132 people

The number who actually took part.

Started

Dec 2024

Finished

Dec 2025

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.

Ages

18 to 75 years

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients undergoing endoscopic submucosal dissection (ESD) at Ningbo University Affiliated First Hospital from December 2024 to December 2026. * Aged between 18 and 75 years. * Patients who voluntarily agree to participate in the study and sign the informed consent form. Exclusion Criteria: * Individuals under 18 years of age. * Patients unwilling or unable to provide informed consent. * Patients with severe chronic cardiac or pulmonary disease, or those who have required hospitalization for coronary or cerebrovascular events or radiotherapy within the past 3 months. * Patients with severe abdominal symptoms such as severe pain, bloating, or nausea. * Patients with inadequate preoperative preparation. * Individuals requiring lifelong anticoagulant therapy, those with severe bleeding disorders, or those who have recently taken anticoagulant or antiplatelet medications. * Pregnant or breastfeeding individuals.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Endoscopic submucosal dissection Endoscopy-assisted Tracheal intubation Video laryngoscope

Contacts and locations

Locations

  • the First Affiliated Hospital of Ningbo University

    Ningbo, Zhejiang, 315000, China

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