Smaller breathing tubes may ease sore throats after thyroid surgery
NCT ID NCT06967896
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests whether using a smaller breathing tube during thyroid surgery can lower the chance of a sore throat afterward. 180 women having thyroid surgery will be randomly assigned to receive a tube with an inner diameter of 6.0, 6.5, or 7.0 millimeters. Researchers will check how many women have a sore throat at 1, 6, 24, and 48 hours after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- tracheal tube (breathing tube) with inner diameters of 6.0mm, 6.5mm, or 7.0mm
- What this could lead to
- If smaller tubes work better, this could lead to a simple change in practice to reduce sore throat after thyroid surgery in women.
- What could go wrong
- This is a small, single-center trial. The benefit may be small or not apply to all patients. There is no new drug or treatment being tested.
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
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About 180 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2025
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- 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.
Who is studied
Healthy female thyroid surgery patients, ages 18-65 years, did not have serious systemic disease
- Ages
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18 to 65 years
- Sex
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Female participants only
- 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.
Show the full entry requirements Hide 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: * Female; * Thyroid surgery should be performed under general anesthesia (GA) at an appropriate time; * ASA grade I-III; * Aged 18-65 years; * BMI less than 35Kg/m2 * In line with ethics, patients voluntarily accept this experiment and sign informed consent. Exclusion Criteria: * Reflux esophagitis, preoperative sore throat, chronic pharyngitis, preoperative hoarseness, use of anticoagulants or corticosteroids, high risk of reflux or aspiration, dysphagia, previous oral or pharyngeal surgical intervention, bleeding disorder, severe heart, lung, liver and kidney dysfunction * Upper respiratory tract infection occurred within 2 weeks before surgery * Unable to insert ET (no more than two intubations) * Patients with hoarseness or sore throat before surgery * Language communication, hearing impairment or brain dysfunction such as stroke, unable to communicate
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
Contacts and locations
Locations
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Department of Anqing Hospital Anesthesiology
RECRUITINGAnqing, Anhui, 246003, China
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