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Simple tube trick may ease sore throat after surgery

NCT ID NCT06218836

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether using a pre-inflated tracheal tube cuff during intubation reduces sore throat after surgery. 250 adults with non-difficult airways were randomly assigned to either the pre-inflated cuff method or the standard deflated cuff method. The goal was to see if reducing friction from the cuff passing through the throat lowers the chance of postoperative sore throat.

What this could mean

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

Active substance
Pre-inflated endotracheal tube cuff
What this could lead to
If it works, this simple technique could reduce sore throat after surgery for many patients.
What could go wrong
This is a single completed study with 250 participants. The technique may not work for everyone or in all surgical settings.

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

250 people

The number who actually took part.

Started

Jan 2024

Finished

Jul 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.

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: * ASA physical status I and II * Patients with anticipated non-difficult airway with the following characteristics: i. Normal head and neck movements ii. Adequate mouth opening iii. No retrognathia or prognathia iv. Normal dentition * Surgeries with anticipated duration of 40 minutes - 3 hours Exclusion Criteria: * Obese patients (BMI \> 33 kg/m2) * Requiring use of intubation aids such as bougie, stylet or video-laryngoscope * Recent history of steroid or non-steroidal anti-inflammatory drug use * Systemic illness with presenting complaints of sore/dry throat (diabetics with polydipsia, hypertensives on diuretics, moribund bed ridden patients) * History of airway related morbidity post operative sore throat \[POST\] * Patients with a history of chronic smoking (1 pack per day for 10 years) chewing tobacco, and tobacco-related products * Patients undergoing head and neck, intraoral/nasal surgery, or recent history of such surgery * Patients with a past surgical history of tracheostomy (post decannulation) * Surgery in prone position * Ongoing upper and lower respiratory tract inflammation/infection * Patients with anticipated postoperative mechanical ventilation * Refusal to participate in the study

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Sir Ganga Ram Hospital

    New Delhi, National Capital Territory of Delhi, 110060, India

More trials for these conditions

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