Study to Evaluate the Safety and Effectiveness of the CODMAN ENTERPRISE® Vascular Reconstruction Device
Public ClinicalTrials.gov record NCT02532517. 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.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Prospective, Multi-center, Single Arm Study to Evaluate the Safety and Effectiveness of the CODMAN ENTERPRISE® Vascular Reconstruction Device and Delivery System When Used in Conjunction With Endovascular Coil Embolization in the Treatment of Wide-necked Saccular Intracranial Aneurysms
Study identification
- NCT ID
- NCT02532517
- Recruitment status
- Terminated
- Study type
- Interventional
- Phase
- Not applicable
- Lead sponsor
- Cerenovus, Part of DePuy Synthes Products, Inc.
- Industry
- Enrollment
- 45 participants
Conditions and interventions
Conditions
Interventions
- CODMAN ENTERPRISE® Vascular Reconstruction Device and Delivery System Device
Device
Eligibility (public fields only)
- Age range
- 21 Years to 70 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
- Aug 31, 2015
- Primary completion
- Jan 7, 2019
- Completion
- Sep 20, 2019
- Last update posted
- Oct 22, 2020
2015 – 2019
United States locations
- U.S. sites
- 11
- U.S. states
- 9
- U.S. cities
- 11
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Radiology Imaging Associates | Englewood | Colorado | 80112 | — |
| University of Florida | Gainesville | Florida | 32611 | — |
| Lyerly Neurosurgery, an Affiliate of Baptist Health | Jacksonville | Florida | 32207 | — |
| University of Illinois at Chicago | Chicago | Illinois | 606012 | — |
| Johns Hopkins University | Baltimore | Maryland | 21287 | — |
| University of Massachusetts Medical Center | Worcester | Massachusetts | 01655 | — |
| University of Buffalo | Buffalo | New York | 14203 | — |
| Mount Sinai Health System | New York | New York | 10029 | — |
| Miami Valley Hospital | Dayton | Ohio | 45409 | — |
| Lehigh Valley Health Network | Allentown | Pennsylvania | 18103 | — |
| Inova Fairfax Hospital | Falls Church | Virginia | 22042 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT02532517, 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 Oct 22, 2020 · Synced Jul 22, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT02532517 live on ClinicalTrials.gov.