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New study tests simple way to cut Post-Surgery sore throat

NCT ID NCT07485972

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 continuously monitoring the pressure of the breathing tube during laparoscopic surgery can reduce airway problems like sore throat, cough, and hoarseness after the operation. 95 adults having elective laparoscopic abdominal surgery were randomly assigned to one of three cuff pressure monitoring methods. The goal was to see if continuous monitoring leads to fewer complications compared to checking pressure every 30 minutes or using a standard cuff-leak technique.

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 lead to a simple change in how breathing tubes are managed during surgery to reduce patient discomfort afterward.
What could go wrong
This is a small, completed study with only 95 participants, so results may not apply to all surgeries or patients. The findings are about symptom reduction, not a cure or major treatment.

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

95 people

The number who actually took part.

Started

May 2024

Finished

Nov 2024

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 65 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 aged 18-65 years * ASA physical status I-II * Scheduled for elective laparoscopic abdominal surgery under general anesthesia * Expected surgery duration longer than 90 minutes Exclusion Criteria: * Predicted difficult airway * Recent upper respiratory tract infection * Preoperative laryngopharyngeal symptoms * Recent endotracheal intubation * Body mass index \> 40 kg/m² * Substance abuse * History of bronchospasm * Tracheostomy * History of laryngeal disease or laryngeal surgery * ASA physical status ≥ III

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Cukurova University Faculty of Medicine, Department of Anesthesiology and Reanimation

    Adana, Adana, 01330, Turkey (Türkiye)

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