Aspirin's secret weapon against preeclampsia? immune cells under the microscope
NCT ID NCT04974892
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study investigated why low-dose aspirin helps prevent preeclampsia in some high-risk pregnant women but not others. Researchers took blood samples from 35 women at four points during pregnancy to study their immune cells, particularly neutrophils. The goal was to identify differences between women who responded to aspirin and those who still developed preeclampsia, which could lead to better prevention strategies.
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 research could help explain why low-dose aspirin prevents preeclampsia in some high-risk women but not others, potentially leading to better prevention strategies.
- What could go wrong
- This is a small observational study (35 participants) that only looks at immune markers, not a treatment trial. The findings may not apply to all women or lead to immediate changes in care.
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
-
35 people
The number who actually took part.
- Started
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Apr 2022
- Finished
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Dec 2025
- 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
Patients at high risk of developing preeclampsia in pregnancy who are started on low dose aspirin at ≤16 weeks.
- Ages
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18 years and older
- Sex
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Female 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.
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 18-60 years * Singleton pregnancy * Live fetus at 11-13 weeks of gestation * Informed, written consent * Upper age of 60 years * Patient taking low dose aspirin as standard of care Exclusion criteria * Unwilling or unable to give consent * Participants who are unable to understand written English
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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.
Contacts and locations
Locations
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Barts Health NHS Trust, The Royal London Hospital
London, E1 1BB, United Kingdom
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Other studies related to the condition(s) this trial covers.
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