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Noninvasive Evaluation for Carotid Artery Stenosis: The Carotid Stenotic Scan

Noninvasive Evaluation for Carotid Artery Stenosis: The Carotid Stenotic Scan

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04057183
Acronym
CSS
Enrollment
300
Registered
2019-08-15
Start date
2019-07-01
Completion date
2020-06-30
Last updated
2019-08-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carotid Stenosis

Keywords

Carotid, Stenosis, Noninvasive

Brief summary

The purpose of this study is to determine the accuracy of a new non-invasive device, the Carotid Stenotic Scan (CSS), to check for stenosis of the internal carotid artery (ICA) as compared to a carotid duplex ultrasound study.

Detailed description

Currently, carotid duplex ultrasound is the primary diagnostic tool for the evaluation for ICA stenosis and must be performed by a trained and certified vascular technologist using advanced duplex imaging equipment and with subsequent interpretation by a trained physician. this test is not considered suitable for screening for disease. It would be of value to develop an accurate, reliable, low-cost, and easily accessible tool to screen for extra-cranial ICA disease in an office based setting. However, such a tool would require novel technology that allows for quick, accurate, reproducible, and safe evaluation. This study will evaluate a new technology called the Carotid Stenotic Scan (CSS) developed by CVR Medical. The CSS instrument uses sensitive transducers to detect low frequency pressure fluctuations associated with flow disturbances downstream from areas of arterial narrowing. Subjects will undergo a clinically ordered clinical carotid duplex ultrasound as part of standard of care. Subjects will have a noninvasive CSS assessment either before or after the carotid duplex ultrasound.

Interventions

DIAGNOSTIC_TESTCarotid Stenotic Scan

Noninvasive determination of presence or absence of carotid artery stenosis

Sponsors

Phillip J Bendick
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients age ≥ 65 years scheduled for a diagnostic carotid artery duplex ultrasound study AND with one or more of the following: * Hypertension * Hyperlipidemia * Diabetes * Tobacco usage - Current or past * Known CAD/PAD * Family history of early onset of atherosclerotic disease

Exclusion criteria

* Unable / unwilling to provide Informed Consent * Prior carotid endarterectomy or carotid artery stent * Aortic stenosis * Congestive heart failure * BMI \> 35

Design outcomes

Primary

MeasureTime frameDescription
Comparison of CSS result to carotid artery duplex ultrasound examinationCSS and duplex ultrasound done within one week of each otherPercent agreement and negative predictive value of CSS compared to duplex ultrasound

Countries

United States

Contacts

Primary ContactPhillip J Bendick, PhD
pbeninnc@gmail.com2483960314
Backup ContactTony Robinson
tonyrobinson@cvrmed.com8105778555

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026