Does the setting of care affect whether kids finish their antibiotics?
NCT ID NCT07711756
First seen Jul 17, 2026 · Last updated Jul 17, 2026
Summary
This observational study looks at whether children aged 3 months to 16 years are more likely to complete their full course of antibiotics when prescribed at a primary care clinic versus a hospital emergency department. Researchers surveyed parents by phone after treatment ended to see if at least 80% of the prescribed antibiotics were taken. The goal is to understand how the healthcare setting might influence treatment adherence.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 191 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2028
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
Pediatric patients presenting to the Gignac Primary Care Health Center or the Pediatric Emergency Department of Montpellier University Hospital with a suspected bacterial infection and considered eligible for an outpatient oral antibiotic prescription.
- Ages
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3 months to 16 years
- 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: * Children aged 3 months to 16 years * Receiving an outpatient oral antibiotic prescription * Diagnosed with an acute bacterial infection Exclusion Criteria: * Unemancipated minors presenting without a parent or legal guardian. * Participation in another clinical research study with an ongoing exclusion period * Refusal to participate after the reflection period * Parents unable to understand the study information (e.g., language barrier or cognitive impairment) * Not affiliated with, or not a beneficiary of, a national health insurance scheme * Pregnant or breastfeeding female participants
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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 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.
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Other studies related to the condition(s) this trial covers.
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