Eye rosacea study seeks safer antibiotic use
NCT ID NCT05296837
First seen Jun 24, 2026 · Last updated Aug 21, 2026 · Updated 5 times
Summary
This study looks at how different doses of the antibiotic doxycycline affect antibiotic resistance in people with ocular rosacea, an inflammatory eye condition. Researchers will compare a low anti-inflammatory dose (40 mg daily) with a standard antibiotic dose (200 mg daily) and a placebo. The goal is to see which dose causes the least resistance in gut bacteria, helping guide safer long-term treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- doxycycline
- What this could lead to
- If successful, this study could help doctors choose the safest doxycycline dose for ocular rosacea, reducing the risk of antibiotic resistance.
- What could go wrong
- This is a small, early-phase study focused on measuring resistance, not on treating symptoms. Results may not change current practice directly.
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
-
46 people
The number who actually took part.
- Started
-
Jun 2023
- Finished
-
Jul 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.
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: * Have symptomatic ocular disease attributed to ocular rosacea as the primary diagnosis * Ability to give informed consent * Be aged 18 years old or older Exclusion Criteria: * Have an active ocular or systemic infection * Have a known allergy or intolerance to tetracycline antibiotics * Have had prior use of oral antibiotics within the last three months * Pregnancy or the possibility of becoming pregnant within the 8-week study medication timeline.
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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
-
University of California, San Farncisco
San Francisco, California, 94143, United States
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