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Nurse-Led sedation for endoscopy proves safe in massive trial

NCT ID NCT06712264

Knowledge-focused Sponsor: The Affiliated Hospital of Qingdao University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether specially trained anesthesia nurses can safely manage sedation for digestive endoscopy, with an anesthesiologist available if needed. Over 18,000 people took part to compare safety and satisfaction. The goal was to see if this nurse-led model could be a safe and effective way to provide painless procedures.

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

18,000 people

The number who actually took part.

Started

Dec 2024

Finished

Feb 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.

Who is studied

Population undergoing gastrointestinal endoscopy examination at Qingdao University Affiliated Hospital from December 2024 to February 2025.

Ages

16 years and older

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: * Age ≥ 16 years old, * no oral intake before surgery: liquid for 2 hours, solid for 6 hours. Exclusion Criteria: * American Society of Anesthesiology (ASA) classification greater than III, * sleep apnea, * allergies to soybeans, eggs, or peanuts, * pregnancy, * previous anesthesia related complications,, * potential difficult ventilation, * acute gastrointestinal bleeding, * sub intestinal obstruction, * severe chronic obstructive pulmonary disease (COPD)

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Conditions

The condition(s) this trial relates to.

agnosia

As listed by the trial registrant

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

Endoscopy, gastrointestinal Pain management

Contacts and locations

Locations

  • the Affiliated Hospital of Qingdao University

    Qingdao, Shandong, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.