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TORUS 2 IDE Clinical Study
NCT04130737 · View on ClinicalTrials.gov ↗
Study Summary
The primary objective of the TORUS 2 IDE Clinical Study is to evaluate the safety and effectiveness of the TORUS Stent Graft System in the treatment of obstructive atherosclerotic lesions of the native SFA or the superficial femoral and/or proximal popliteal arteries.
Conditions Studied
Interventions
- DEVICE TORUS Stent Graft System
Study Locations (20)
Arizona
- Southwest CVA — Mesa
- Vascular Heart & Lung Associates — Mesa
- Phoenix Cardiovascular Research Group — Phoenix
- Yuma Cardiology Associates — Yuma
Florida
- First Coast Cardiovascular Institute — Jacksonville
- Palm Vascular Centers — Miami Beach
- Coastal Vascular & Interventional — Pensacola
- Florida Cardiology — Winter Park
Michigan
- McLaren Bay Region — Bay City
- Michigan Vascular Center — Flint
- Eastlake Cardiovascular — Roseville
California
- Bay Area Vein & Vascular Institute — Burlingame
- UCSF — San Francisco
Arkansas
- Arkansas Heart — Little Rock
Colorado
- Rocky Mountain Regional VAMC — Aurora
Connecticut
- The Vascular Experts — Darien
Illinois
- AMITA Health — Elk Grove
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 188 participants |
| Start Date | 2019-10-31 |
| Est. Completion | 2024-12-24 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04130737
The ClinicalTrials.gov registry entry for NCT04130737 describes a study currently listed as active not recruiting. 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 188 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Endologix, which has 10 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Peripheral Arterial Disease appearing as the primary indexed condition, and to 1 intervention — of which TORUS Stent Graft System 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: NCT04130737 reports 20 study locations spanning 11 distinct geographic areas — top geographies include Arizona, Florida, Michigan. 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 NCT04130737 about?
NCT04130737 is a clinical study titled "TORUS 2 IDE Clinical Study". The primary objective of the TORUS 2 IDE Clinical Study is to evaluate the safety and effectiveness of the TORUS Stent Graft System in the treatment of obstructive atherosclerotic lesions of the native SFA or the superficial femoral and/or proximal popliteal arteries.
What is the current status of trial NCT04130737?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 188 participants. The study started on 2019-10-31. Estimated completion is 2024-12-24.
What conditions does trial NCT04130737 study?
This clinical trial studies the following conditions: Peripheral Arterial Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04130737?
The interventions under investigation include: TORUS Stent Graft System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04130737?
This trial is sponsored by Endologix, which has 10 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04130737 being conducted?
This trial has 20 study locations across Arizona, Arkansas, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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