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Does a simple tool beat the old thumb trick for breathing tubes?

NCT ID NCT07427173

Knowledge-focused Sponsor: University of Gaziantep Source: ClinicalTrials.gov ↗

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looks at 104 adults having surgery with a breathing tube. It compares using a special pressure gauge (manometer) versus the traditional finger-pinch method to set the tube's cuff pressure. The goal is to see if the gauge reduces sore throat, hoarseness, or other airway problems after surgery.

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 104 people

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

Expected to start

Feb 2026

An estimate. Start dates often move.

Expected to finish

Sep 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

The study population will consist of adult patients aged 18-75 years, classified as American Society of Anesthesiologists (ASA) physical status I-III, with a body mass index between 18 and 30 kg/m², who are scheduled to undergo elective surgery under general anesthesia requiring endotracheal intubation. Only patients with successful intubation on the first attempt will be included.

Ages

18 to 75 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: * Patients aged 18-75 years * American Society of Anesthesiologists (ASA) physical status I-III * Body mass index (BMI) between 18 and 30 kg/m² * Undergoing surgery under general anesthesia * Successful endotracheal intubation on the first attempt -Provided written informed consent and willing to participate in the study- Exclusion Criteria: * Patients younger than 18 years or older than 75 years * American Society of Anesthesiologists (ASA) physical status IV-VI * Patients undergoing head and neck surgery * History of chronic pulmonary disease (e.g., asthma, chronic obstructive pulmonary disease) * Presence of preoperative sore throat * History of upper or lower respiratory tract infection within the past 2 weeks * Use of systemic steroids in the preoperative period * More than one attempt required for endotracheal intubation * Emergency surgeries * Refusal to participate in the study

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As listed by the trial registrant

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

Postoperative airway complications

How to take part

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  1. 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.

    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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