Pumping every 2 hours may boost milk supply for preemie moms
NCT ID NCT06673160
First seen Jun 27, 2026 · Last updated Jul 17, 2026 · Updated 2 times
Summary
This study looks at whether pumping breast milk every 2 hours instead of every 3 hours helps mothers of preterm babies produce more milk. About 70 mothers will be assigned to one of two pumping schedules and record their daily milk volume for the first 28 days after birth. The goal is to find the best pumping frequency to support milk supply.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- breast pumping (every 2 or 3 hours)
- What this could lead to
- If it works, this could help mothers of preterm babies produce more breast milk, reducing the need for donor milk.
- What could go wrong
- This is a small, early-stage study (70 participants) that only measures milk volume, not long-term health outcomes. Results may not apply to all mothers.
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 70 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2025
- Expected to finish
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Dec 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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Up to 28 days
- 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: * Inborn infants \<32 weeks gestation * Out-born infants transferred to our facility \<48hours of life * Infants \<1500 grams at birth * Infants whose parents/ guardians have provided legal consent for study participation Exclusion Criteria: * Infants with birthing persons' that are severe/critically ill * Birthing persons of infants \<18 years old * Infants with terminal illness or decision to withhold or limit support * infants with major congenital anomalies, chromosomal disorders, or congenital infections
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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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University of Alabama Birmingham
RECRUITINGBirmingham, Alabama, 35249, United States
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