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New device aims to keep obese patients breathing safely during endoscopy

NCT ID NCT06796764

First seen Nov 01, 2025 · Last updated Jun 23, 2026 · Updated 29 times

Summary

This study tests a new device called the COMBO Endoscopy Oropharyngeal Airway in 580 obese patients undergoing gastrointestinal endoscopy under sedation. The device combines oxygen delivery, airway support, and monitoring to prevent low oxygen levels, a common risk in these patients. Half the participants will use the new device, while the other half will receive standard oxygen via a nasal cannula.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • The First Affiliated Hospital, Zhejiang University School of Medicine

    RECRUITING

    Hangzhou, Zhejiang, 310000, China

    Contact Phone: •••-•••-•••• Email: •••••@•••••

  • The Fourth Affiliated Hospital, Zhejiang University School of Medicine

    RECRUITING

    Hangzhou, Zhejiang, 310000, China

    Contact Phone: •••-•••-•••• Email: •••••@•••••

  • Zhejiang Cancer hospital

    RECRUITING

    Hangzhou, Zhejiang, 310000, China

    Contact Phone: •••-•••-•••• Email: •••••@•••••

What this could mean

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

Active substance

COMBO Endoscopy Oropharyngeal Airway device

What this could lead to

If it works, this device could reduce the risk of dangerously low oxygen levels during routine endoscopy in obese patients, making the procedure safer.

What could go wrong

This is an early-stage device trial with no phase designation. The device may not perform better than standard care, and results may not apply to all patients or settings.

Conditions

The condition(s) this trial relates to.

Esophageal Neoplasms gastric neoplasm Hypoxia

As listed by the trial registrant

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