Simple tube trick may ease sore throat after surgery
NCT ID NCT06218836
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
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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
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250 people
The number who actually took part.
- Started
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Jan 2024
- Finished
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Jul 2025
- Lead sponsor
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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
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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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
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Sir Ganga Ram Hospital
New Delhi, National Capital Territory of Delhi, 110060, India
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Other studies related to the condition(s) this trial covers.
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