Tiny plastics, big questions: new study probes microplastic risks for infants
NCT ID NCT06107933
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This observational study at Johns Hopkins looks at microplastic exposure in 40 mother-infant pairs in Baltimore. Researchers will test breastmilk, maternal blood, and infant stool for tiny plastic particles. They also track infant weight, length, and growth to see if microplastics are linked to development. The goal is to understand what plastics are present and how they might affect early life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could reveal how microplastics enter infants' bodies and whether they affect growth, pointing to ways to reduce exposure.
- What could go wrong
- This is a small observational study with only 40 participants, so findings may not apply to everyone. It measures exposure but cannot prove microplastics cause health problems.
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.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2023
- Expected to finish
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Jan 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.
Who is studied
The study will include 20 mother-infant pairs from Baltimore City and County. We will be studying lactating mothers at 1 or 3 months postpartum ±2 weeks.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * All gender expressions * Mothers at 1 or 3 months postpartum (± 2 weeks) * Intent to exclusively breastfeed for ≥ 6 months * Nulliparous and singleton births * Receiving only breast milk from the mother, with no formula supplementation Exclusion Criteria: * Physical, mental, or cognitive disability that prevents participation; current incarceration * Chronic conditions in mother and/or infant (e.g., heart disease, cancer, autoimmune disease, diabetes, intestinal bowel syndrome/disease), conditions diagnosed for the first time during pregnancy (e.g. gestational diabetes), neurological conditions in mother and/or infant (e.g. epilepsy, seizures), psychological conditions in mother and/or infant (e.g. bipolar disorder), or neurological/psychological conditions diagnosed in mother during or immediately after pregnancy (e.g. postpartum depression) * Previously diagnosed with any major illness (e.g., intrauterine growth restriction, birth asphyxia, cancer) or eating disorder or previous gastric band surgery * Maternal antibiotic use during pregnancy or the postpartum period. Infant antibiotic use at any time during life or taking medications that could affect plastic exposure or the microbiome, such as medications administered via a plastic syringe. * Use of any breast pump except the Silicon Breast Pump for the 14 days prior to the clinical visit. * PHQ9 score greater than or equal to 10 indicating clinically relevant symptoms of moderate or worse depression * Infants who are intersex * Smoking, drug use (including marijuana use), or alcohol abuse
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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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East Baltimore Pediatric Inpatient and Outpatient Clinical Research Unit
RECRUITINGBaltimore, Maryland, 21287, United States
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