Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

Measuring Blood Pressure in Pregnant Women Using Different Cuffs

Official title: Evaluation of the Agreement Between Conical Forearm and Cylindrical Upper Arm Non-Invasive Blood Pressure (NIBP) Measurements in Pregnant Patients

Run by Northwestern University · NCT06466161 · Data updated 2026-11-12

This study is testing if a special forearm cuff gives more accurate blood pressure readings for pregnant women compared to a regular upper arm cuff, especially for those who are very overweight.

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Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment110 (estimated)
SponsorNorthwestern University
Academic / other
Locations1 site (Chicago, Illinois)
StatusRecruiting
StartedApril 29, 2025
Main results expectedJuly 30, 2027
Study endsSeptember 1, 2027
Registry record updatedMay 26, 2026
Trial IDNCT06466161 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are pregnant women aged 18 and older with a BMI of 20 kg/m² or greater, presenting with or without a diagnosis of hypertension.

Probably not a fit

Patients with significant peripheral arterial disease or a history of certain heart conditions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the accuracy of blood pressure measurements in pregnant women using two different types of cuffs: a cylindrical cuff for the upper arm and a conical cuff for the forearm. Participants will be categorized into four groups based on their blood pressure and obesity status. The goal is to determine if the conical cuff provides more accurate readings, especially in morbidly obese patients, which could lead to better diagnosis and management of hypertension during pregnancy. Measurements will be taken while participants are seated, and various arm and forearm dimensions will be recorded to ensure proper cuff fitting.

Why it matters

Potential benefit: If successful, this study could lead to more accurate blood pressure readings in pregnant women, reducing unnecessary treatments and complications.

How similar studies have gone: Other studies have indicated that improved cuff designs can enhance blood pressure measurement accuracy, suggesting potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Women who are 18 years of age or older with a
* Body mass index (BMI) of 20 kg/m2 or greater
* Present to Labor and Delivery with or without a diagnosis of gestational hypertension, preeclampsia, or chronic hypertension with super-imposed preeclampsia, in spontaneous labor or for induction of labor

Exclusion Criteria:

* Significant peripheral arterial disease resulting in at least a 10 mm Hg blood pressure difference between both arms
* History of repaired or unrepaired congenital heart disease
* History of significant arrythmia
* History of pacemaker or implantable cardioverter defibrillator placement
* History of sickle cell disease
* History of Raynaud's phenomenon on any extremity
* History of lymph node dissection of either upper extremity
* Patients who are less than 18 years of age

Where it's running

  • Prentice Women's Hospital
    Chicago, Illinois, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.