Ankle cuff could let moms hold baby Skin-to-Skin right after C-Section
NCT ID NCT07422766
First seen Jun 25, 2026 · Last updated Aug 07, 2026 · Updated 2 times
Summary
This study checks if blood pressure readings from an ankle cuff are as accurate as those from a standard arm cuff during planned C-sections. About 110 women will have their blood pressure measured at both sites. If ankle readings are reliable, mothers could hold their newborns skin-to-skin right after birth without needing an arm cuff in the way.
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 could show that ankle blood pressure cuffs are reliable during C-sections, allowing mothers to hold their babies skin-to-skin right after birth without removing the cuff.
- What could go wrong
- This is a small observational study, not a treatment trial. The results may not apply to all patients or situations, and ankle readings might not match arm readings closely enough for routine use.
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 110 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Dec 2026
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 target population will be adult pregnant women scheduled for elective cesarean delivery at CHU Sainte-Justine.
- 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: * Women scheduled for elective cesarean under neuraxial anesthesia at CHU Sainte-Justine. * American Society of Anesthesiologists Physical Status I-III * Singleton pregnancy * Gestation ≥ 35 weeks * BMI \< 40 * Able to consent in French or English Exclusion Criteria: * Cesarean planned under general anesthesia. * Multiple pregnancy * Prematurity \< 35 weeks gestation * Major fetal anomalies * Morbid obesity (BMI ≥ 40) * Active labor * Emergency cesarean * Prisoners * Peripheral vascular disease requiring medication or treatment * Hypertensive diseases requiring medication * Inability to place blood pressure cuff on ankle (amputation, dysmorphism, etc.) * Complications requiring significant hemodynamic support (transfusions, inotropes, multiple vasopressors, etc.
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Genom att skicka in godkänner du våra Användarvillkor
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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CHU Sainte-Justine
RECRUITINGMontreal, Quebec, H3T 1C5, Canada
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