Can a squirt of medicine in the windpipe stop coughing after sinus surgery?
NCT ID NCT07504497
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares two drugs, dexmedetomidine and lidocaine, sprayed into the windpipe to see which one reduces coughing better when patients wake up from sinus or nose surgery. 120 adults having elective sinus surgery will take part. The goal is a smoother, more comfortable recovery from anesthesia.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- dexmedetomidine
- What this could lead to
- If it works, this could offer a simple way to reduce coughing and discomfort when waking up from sinus surgery.
- What could go wrong
- This is a small, early-phase study (120 people) comparing two drugs; results may not apply to other surgeries or patients with lung problems.
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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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 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.
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * \- Age 18-60 years. * Elective FESS under general anesthesia. * ASA Physical Status I-II Exclusion Criteria: * Allergy to dexmedetomidine or lidocaine * Anticipated difficult airway * Chronic pulmonary diseases (asthma, COPD) * Uncontrolled hypertension or ischemic heart disease * Patient refusal
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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 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.