Shorter antibiotic course may be just as effective for kids with pneumonia
NCT ID NCT07647835
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a 3-day course of amoxicillin works as well as a 5-day course for children aged 3 months to 5 years with uncomplicated pneumonia. The goal is to see if shorter treatment can reduce side effects, lower costs, and fight antibiotic resistance. About 250 children will take part, and their recovery will be checked at day 14.
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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Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
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About 250 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2027
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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3 months to 5 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.
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; ≥ 3 months to 5 years * Fever; recorded temperature of ≥100.4 f or guardian reported fever within 2 days * Cough; observed or reported within 3 days * Tachypnea; * 3 months to 1 years ≥ 50 breaths per minute * 1 years to 5 years ≥ 40 breaths per minute * C- reactive protein ≥ 40 * White blood cells ≥ 12200 * Chest X-ray; * Presence of a dense opacity occupying a portion or whole of lobe with or without air Broncho grams. Exclusion criteria: * Patient who is Lethargic and unable to tolerate orally. * Capillary refill greater than 2 second * Chronic lung disease * Congenital heart disease or sickle cell anemia patient * Immunocompromised patient * malnourished * Known or suspected tuberculosis patient * Patient has used prior antibiotic within 2 days * Allergic to penicillin or amoxicillin * C-reactive protein greater than 72 * White blood cells greater than 25000 * Chest x rays show linear or patchy or peri bronchial opacity * Presence of pleural effusions * Empyema, lung abscess, necrotizing pneumonia or pneumatocele * Other alternative diagnosis like wheezing syndrome (Bilateral wheezing on auscultation)
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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 places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Khyber Teaching Hospital
Peshawar, Khyber Pakhtunkhwa, 25000, Pakistan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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