Could a light zap in the nose stop deadly ICU infections?
NCT ID NCT06867458
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new method to prevent serious lung and bloodstream infections in intensive care unit (ICU) patients. The treatment uses a special light and a blue dye to kill germs in the nose. Researchers enrolled 227 adults in the ICU and checked if the procedure was practical and reduced infection rates. The goal was to gather information for a larger, more definitive study.
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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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227 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Dec 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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19 years and older
- 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: * All ICU patients 19 years and above * Expected length of ICU stay \>48 hrs Exclusion Criteria: * Pregnant/breastfeeding individuals * Allergy to methylene blue and/or chlorhexidine gluconate, or unknown allergy status * Nasal or facial trauma that limits access to the nose * Inability for the patients to tolerate or comply with treatment, as determined by their treating physician * Patient, TSDM or MRP declines participation * Co-enrolment with other research studies will be considered in an individual basis.
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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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Royal Columbian Hospital
New Westminster, British Columbia, V3L 3W7, Canada
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Other studies related to the condition(s) this trial covers.
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