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Clinical Trials in Canada / NCT07422766
Recruiting Observational

Comparison of Non-Invasive Mean Arterial Blood Pressure Measurements at the Arm and Ankle During Elective Cesarean Delivery.

NCT07422766 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2026-02-26
Last updated
2026-08-07

Condition(s) studied

PregnancyCesarean DeliveryBlood Pressure Measurement in PregnancySkin to Skin Contact

Investigational drug(s) / intervention(s)

Mean arterial pressure

Mean arterial pressure: Mean arterial pressure will be taken on the arm and on the ankle from the same patient and compared.

Study summary

This observational study aims to compare mean arterial pressure measurements obtained using an ankle blood pressure cuff with those obtained using a standard upper-arm cuff in pregnant individuals undergoing elective cesarean delivery under spinal anesthesia. The primary objective is to determine the level of agreement between the two measurement sites.The main question\[s\] it aims to answer \[is/are\]:

Demonstrate that the mean arterial pressure is similar between arm and ankle with the blood pressure cuff

Every participant will be their own control. (Measurements will be taken at both sites on every participant)

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CHU Sainte-Justine Montreal Quebec Recruiting

More St. Justine's Hospital trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07422766 on ClinicalTrials.gov ↗ ← All trials in Canada