Heart monitoring reveals best position for uterus during C-Section
NCT ID NCT02283931
First seen Jul 13, 2026 · Last updated Jul 14, 2026 · Updated 1 time
Summary
This study uses two noninvasive heart-monitoring tools—ultrasound and a special monitor—to measure how different positions of the uterus affect a pregnant woman's blood flow. Researchers will compare three standard uterine displacement techniques in healthy women at full term who are not in labor. The goal is to find out which position best supports the mother's heart function, which could help guide anesthesia care during cesarean deliveries.
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 one position is found to improve blood flow, it could guide safer anesthesia care for cesarean sections.
- What could go wrong
- This is a small observational study with 25 healthy pregnant women, so results may not apply to all pregnancies or those with complications.
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 25 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2015
- 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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18 to 50 years
- 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: 1. Healthy ASA physical status I-II 2. Term parturient Exclusion Criteria: 1. Woman in labor 2. Presence of maternal medical conditions affecting the cardiovascular system (including preeclampsia, gestational hypertension) 3. Fetal anomaly or intrauterine growth restriction (\< 25th percentile) 4. Maternal renal or endocrine disease
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States