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PRESERVE-Zenith® Iliac Branch System Clinical Study
NCT01208415 · View on ClinicalTrials.gov ↗
Study Summary
The PRESERVE-Zenith® Iliac Branch System Clinical Study is a clinical trial to study the safety and effectiveness of the Zenith® Branch Endovascular Graft-Iliac Bifurcation in combination with the Zenith® Connection Endovascular Stent/ConnectSX™ covered stent in the treatment of aorto-iliac and iliac aneurysms.
Conditions Studied
Interventions
- DEVICE Endovascular repair for aortoiliac or iliac aneurysms.
Study Locations (19)
Pennsylvania
- Hospital of the University of Pennsylvania — Philadelphia
- Allegheny General Hospital — Pittsburgh
- University of Pittsburgh Medical Center — Pittsburgh
California
- VA Palo Alto HCS — Palo Alto
- Stanford University Medical Center — Stanford
Florida
- Christine E. Lynn Heart and Vascular Institute — Boca Raton
- University of Florida — Gainesville
Missouri
- Washington University School of Medicine — St Louis
- Mercy Hospital East Communities — St Louis
New York
- Columbia University Medical Center — New York
- Weill Cornell Medical Center — New York
Georgia
- Emory University — Atlanta
Massachusetts
- University of Massachusetts — Worcester
Michigan
- William Beaumont Hospital — Royal Oak
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2011-01 |
| Est. Completion | 2017-10-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01208415
The ClinicalTrials.gov registry entry for NCT01208415 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cook Group Incorporated, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Aorto-iliac Aneurysms appearing as the primary indexed condition, and to 1 intervention — of which Endovascular repair for aortoiliac or iliac aneurysms. is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT01208415 reports 19 study locations spanning 13 distinct geographic areas — top geographies include Pennsylvania, California, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT01208415 about?
NCT01208415 is a clinical study titled "PRESERVE-Zenith® Iliac Branch System Clinical Study". The PRESERVE-Zenith® Iliac Branch System Clinical Study is a clinical trial to study the safety and effectiveness of the Zenith® Branch Endovascular Graft-Iliac Bifurcation in combination with the Zenith® Connection Endovascular Stent/ConnectSX™ covered stent in the treatment of aorto-iliac and ilia...
What is the current status of trial NCT01208415?
This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2011-01. Estimated completion is 2017-10-10.
What conditions does trial NCT01208415 study?
This clinical trial studies the following conditions: Aorto-iliac Aneurysms, Iliac Aneurysms. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01208415?
The interventions under investigation include: Endovascular repair for aortoiliac or iliac aneurysms. (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01208415?
This trial is sponsored by Cook Group Incorporated, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01208415 being conducted?
This trial has 19 study locations across California, Florida, Georgia, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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