CompletedPhase 1

Acetaminophen Transfer Across the Placenta and the Assessment of Fetal Well-being

United States56 participantsStarted 2010-09

Plain-language summary

This study has two aims: 1. to evaluate placental transfer of acetaminophen from mother to baby transplacentally given from 30 minutes to 24 hours prior to cesarean delivery (34 patients) 2. to understand the impact of maternal acetaminophen use on fetal movement and breathing (20 patients)

Who can participate

Age range

18 Years – 44 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria * Pregnant females * Age 18-44 * Any race * Any parity * Singleton Gestations * Weight between 60-90 kg Exclusion Criteria * Acetaminophen Allergy * Contraindication to Acetaminophen Use * Chorioamnionitis * Preeclampsia * Diabetes Mellitus * Placental Abruption * Placenta Previa * Fetal Anomaly * Intrauterine growth restriction (IUGR) * Multiple Gestations * Maternal Medical Disease * Acetaminophen use in the last 3 days * Plan to donate or bank fetal cord blood

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Maternal and neonatal serum acetaminophen level

Timeframe: Time Frame: 30 minutes to 24 hours post administration

Fetal breathing and body movements

Timeframe: Time Frame: 60 minutes

Trial details

NCT IDNCT01211912

SponsorMayo Clinic

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2011-12

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