Coconut oil vs. antibiotic ointment: which helps babies heal better after circumcision?
NCT ID NCT07750093
First seen Aug 06, 2026 · Last updated Aug 12, 2026 · Updated 3 times
Summary
This trial compares two post-circumcision care options for infants: an antibiotic ointment called Polyfax and coconut oil. The goal is to see which leads to fewer complications like bleeding, infection, or delayed healing, and which parents find more satisfactory. About 90 infants under 6 months old will be randomly assigned to one of the two treatments, and they'll be checked at 1 week, 3 months, and 6 months after the procedure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Polyfax (antibiotic ointment) or coconut oil applied locally after circumcision
- What this could lead to
- If one works better, it could point to a simpler, safer routine for infant circumcision care, reducing complications and improving healing.
- What could go wrong
- This is a small, early-stage trial, so results may not apply broadly. Also, individual reactions to either substance could vary, and the study doesn't compare against no treatment.
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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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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About 90 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Oct 2026
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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1 week to 6 months
- Sex
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Male participants only
- 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 male patients undergoing Plastibell circumcision \<6m of age, whose parents/ guardians have given consent Exclusion Criteria: * Patient with a known coagulation disorder * Immunosuppressed patients * Patients with a dermatologic condition * Non-compliant patients
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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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Liaquat National Hospital
Karachi, Pakistan
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