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.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 110 (estimated) |
| Sponsor | Northwestern University Academic / other |
| Locations | 1 site (Chicago, Illinois) |
| Status | Recruiting |
| Started | April 29, 2025 |
| Main results expected | July 30, 2027 |
| Study ends | September 1, 2027 |
| Registry record updated | May 26, 2026 |
| Trial ID | NCT06466161 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
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Prentice Women's Hospital
Chicago, Illinois, United States Recruiting
Study contacts
- Principal investigator: Adithya Bhat, MD — Northwestern University
- Study coordinator: Adithya Bhat, MD
- Email: adithya.bhat@northwestern.edu
- Phone: 312-472-3585
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.