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Active, not recruiting Not applicable Interventional

Safety and Efficacy of the CGuard™ Carotid Stent System in Carotid Artery Stenting

ClinicalTrials.gov ID: NCT04900844

Public ClinicalTrials.gov record NCT04900844. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 1:17 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Single-Arm, Pivotal Study to Evaluate the Safety and Efficacy of the CGuard™ Carotid Stent System When Used to Treat Symptomatic and Asymptomatic Carotid Artery Stenosis in Patients Undergoing Carotid Artery Stenting

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this pivotal study is to evaluate the safety and efficacy of the CGuard™ Carotid Stent System in the treatment of carotid artery stenosis in symptomatic and asymptomatic patients undergoing carotid artery stenting (CAS) to a performance goal developed from published CAS literature.

Study identification

NCT ID
NCT04900844
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
InspireMD
Industry
Enrollment
317 participants

Conditions and interventions

Eligibility (public fields only)

Age range
19 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 1, 2021 (Actual)
Primary completion
Jul 1, 2022 (Actual)
Completion
Oct 1, 2025 (Estimated)
Last update posted
Apr 4, 2025

2021 – 2025

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
University of Florida Jacksonville Florida 32209 —
Oschner Health New Orleans Louisiana 70121 —
Ascension, St. John Hospital Detroit Michigan 48236 —
Mercy Hospital St Louis Missouri 63141 —
University of Buffalo Buffalo New York 14203 —
Columbia University Irving Medical Center New York New York 10032 —
Stony Brook University Hospital Stony Brook New York 11794 —
Novant Health Winston-Salem North Carolina 27103 —
Cleveland Clinic Cleveland Ohio 44103 —
UPMC-Pinnacle Harrisburg Pennsylvania 17101 —
Miriam Hospital Providence Rhode Island 02906 —
Prisma Health-Upstate Greenville South Carolina 29605 —
Avera Heart Hospital Sioux Falls South Dakota 57108 —
Ballad CVA Heart Institute Kingsport Tennessee 37660 —
Turkey Creek Medical Center Knoxville Tennessee 37934 —
Ascension Seton, Seton Heart Institute Austin Texas 78705 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04900844, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 4, 2025 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04900844 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →