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Completed Not applicable Interventional Results available

Cerebral Protection in Transcatheter Aortic Valve Replacement

ClinicalTrials.gov ID: NCT02214277

Public ClinicalTrials.gov record NCT02214277. 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 24, 2026, 1:33 AM EDT

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

Official title

Cerebral Protection in Transcatheter Aortic Valve Replacement - The SENTINEL Study

Brief summary

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

The Sentinel System will be a safe and effective method for capturing and removing embolic material (thrombus/debris) during transcatheter aortic valve replacement in order to reduce the ischemic burden in the cerebral anterior circulation.

Study identification

NCT ID
NCT02214277
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Claret Medical
Industry
Enrollment
363 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Sep 2014 (Type not available)
Primary completion
Mar 2016 (Actual)
Completion
Jun 2016 (Actual)
Last update posted
May 11, 2018

2014 – 2016

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
12
Facility City State ZIP Site status
Cedars-Sinai Medical Center Los Angeles California — —
Washington Hospital Center Washington D.C. District of Columbia — —
Morton Plant Hospital Clearwater Florida — —
Emory University Hospital Atlanta Georgia — —
Henry Ford Hospital Detroit Michigan — —
Barnes-Jewish Hospital St Louis Missouri — —
Columbia University Medical Center New York New York — —
Icahn School of Medicine at Mount Sinai New York New York — —
Weill Cornell Medical Center New York New York — —
Cleveland Clinic Foundation Cleveland Ohio — —
Hospital of the University of Pennsylvania Philadelphia Pennsylvania — —
UT Houston / Memorial Hermann Houston Texas — —
UVA Advanced Cardiac Valve Center Charlottesville Virginia — —
UW Medical Center Seattle Washington — —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02214277, 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 May 11, 2018 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02214277 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →