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New study aims to predict breathing tube removal success

NCT ID NCT07577453

Knowledge-focused Sponsor: Gaziantep City 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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 watches 150 adults having planned surgery to see if combining three monitoring checks—breathing pattern, muscle strength, and brain activity—can better predict when it's safe to remove the breathing tube. Doctors will record these checks before removing the tube and watch for any breathing problems for 30 minutes after. The goal is to find a more accurate way to avoid complications after anesthesia.

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

About 150 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Aug 2026

An estimate. End dates often move.

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

Adult patients undergoing elective surgery under general anesthesia with endotracheal intubation and planned extubation in the operating room will be prospectively enrolled. Patients will be included if pre-extubation RSBI, TOF ratio, and BIS measurements can be obtained and if they provide written informed consent.

Ages

18 to 80 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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 between 18 and 80 years * ASA physical status I-III * Patients scheduled for elective surgery under general anesthesia * Patients undergoing endotracheal intubation during general anesthesia * Patients receiving neuromuscular blocking agents during anesthesia * Patients planned for extubation in the operating room * Availability of pre-extubation RSBI, TOF ratio, and BIS measurements * Written informed consent obtained from the patient Exclusion Criteria: * Emergency surgery * Age \<18 years or \>80 years * ASA physical status IV or higher * Known or anticipated difficult airway * Anticipated difficult extubation * Preoperative mechanical ventilation * Planned postoperative mechanical ventilation or transfer to the intensive care unit while intubated * Known neuromuscular disease * Severe chronic respiratory failure * Severe chronic obstructive pulmonary disease associated with respiratory failure * Significant neurological disease affecting respiratory drive or level of consciousness * Conditions or medications that may interfere with reliable neuromuscular monitoring * Inability to obtain reliable RSBI, TOF ratio, or BIS measurements * Refusal to participate * Incomplete perioperative or post-extubation outcome data

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As listed by the trial registrant

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

Extubation failure Extubation success Postoperative respiratory complications

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. 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.

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