Could a nebulized cocktail make lung scopes less Cough-Inducing?
NCT ID NCT07743333
First seen Aug 03, 2026 · Last updated Aug 04, 2026 · Updated 1 time
Summary
This trial tests whether adding nebulized ketamine to lidocaine before a fiberoptic bronchoscopy reduces coughing and discomfort compared to lidocaine alone or standard spray. About 134 adults scheduled for bronchoscopy will receive one of three premedication approaches. The study tracks cough severity, patient tolerance, satisfaction, and safety, including blood pressure and oxygen levels.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Nebulized lidocaine and ketamine
- What this could lead to
- If effective, this combination could make bronchoscopy more comfortable and safer, reducing coughing and improving patient tolerance during the procedure.
- What could go wrong
- This is a single-center trial with a modest number of participants, and the added benefit of ketamine may be small or come with side effects like sedation or blood pressure changes.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
134 people
The number who actually took part.
- Started
-
Sep 2024
- Finished
-
Feb 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 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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: * All patients were assigned for FOB for diagnostic causes as part of their usual care. * All patients were assigned for FOB for therapeutic causes as part of their usual care. Exclusion Criteria: * unstable angina or recent myocardial infarction, * hypoxemia that is not corrected by oxygen therapy, * increased intracranial pressure or recent cerebrovascular stroke, * uncontrolled uraemia, * uncontrolled hypertension, * current viral infections or colds, * history of allergy to lidocaine or ketamine, * altered mental status, or * non-corrected coagulopathy
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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
-
Alexandria University Faculty of Medicine
Alexandria, Alexandria Governorate, 21526, Egypt
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