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Completed Not applicable Interventional Results available

Safety and Effectiveness of an Intracranial Aneurysm Embolization System for Treating Large or Giant Wide Neck Aneurysms

ClinicalTrials.gov ID: NCT01716117

Public ClinicalTrials.gov record NCT01716117. 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 Jul 22, 2026, 3:13 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

The Surpass Intracranial Aneurysm Embolization System Pivotal Trial to Treat Large or Giant Wide Neck Aneurysms (SCENT Trial)

Study identification

NCT ID
NCT01716117
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Stryker Neurovascular
Industry
Enrollment
213 participants

Conditions and interventions

Conditions

Interventions

  • Surpass Flow Diverter Device

Device

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
Oct 24, 2012
Primary completion
Dec 10, 2016
Completion
Jul 6, 2022
Last update posted
Dec 18, 2022

2012 – 2022

United States locations

U.S. sites
25
U.S. states
17
U.S. cities
24
Facility City State ZIP Site status
University of California Irvine California 92697
Santa Barbara Cottage Hospital Santa Barbara California 93105
University of Florida Gainesville Florida 32611
Lyerly Neurosurgery/Baptist Health System Jacksonville Florida 32207
Mayo Clinic - Florida Jacksonville Florida 32224
Baptist Hospital of Miami Miami Florida 33176
Tampa General Hospital Tampa Florida 33606
Rush University Medical Center Chicago Illinois 60612
The University of Kansas Medical Center Kansas City Kansas 66160
Johns Hopkins University Baltimore Maryland 21287
University of Massachusetts Medical School Worcester Massachusetts 01655
Mayo Clinic - Minnesota Rochester Minnesota 55902
University at Buffalo Buffalo New York 14203
Columbia University New York New York 10032
Cleveland Clinic Cleveland Ohio 44195
Oregon Health and Science University Portland Oregon 97239
Thomas Jefferson University Philadelphia Pennsylvania 19107
Medical University of South Carolina Charleston South Carolina 29425
Fort Sanders Medical Center Knoxville Tennessee 37916
Vanderbilt University Medical Center Nashville Tennessee 37232
University of Texas - Southwestern Dallas Texas 75390
Baylor College of Medicine Houston Texas 77030
University of Utah Salt Lake City Utah 84132
University of Virginia Charlottesville Virginia 22908
The Medical College of Wisconsin Milwaukee Wisconsin 53226

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 NCT01716117, 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 Dec 18, 2022 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01716117 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →