Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING NA

Clinical Study of the Treovance Stent-Graft for Patients With Abdominal Aortic Aneurysms

NCT02009644 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this clinical trial is to assess and evaluate the safety and efficacy of the Treovance Stent-Graft with Navitel Delivery System in subjects with Abdominal Aortic Aneurysms (AAA).

Interventions

  • DEVICE Subjects who receive the Treovance stent-graft

Study Locations (20)

New York

  • Community Care (previously Albany Medical Center) — Albany
  • Buffalo General Medical Center — Buffalo
  • Mount Sinai Medical Center — New York
  • University of Rochester -- Strong Memorial Hospital — Rochester
  • Stony Brook Medical Center — Stony Brook

Illinois

  • Presence Medical Center -- Christie Clinic — Champaign
  • University of Chicago — Chicago
  • Affiliated Surgeons of Rockford Memorial Hospital — Rockford

Massachusetts

  • Tufts University Medical Center — Boston
  • Massachusetts General Hospital — Boston
  • University of Massachusetts — Worcester

North Carolina

  • Mission Hospital — Asheville
  • East Carolina University / Pitt County Memorial Hospital — Greenville

Alabama

  • University of Alabama-Birmingham — Birmingham

Arizona

  • Arizona Heart Institute — Phoenix

Connecticut

  • Danbury Hospital — Danbury

Florida

  • Lynn Heart and Vascular Institute — Boca Raton

Trial Details

FieldValue
Enrollment Target 158 participants
Start Date 2013-11-23
Est. Completion 2026-06
Phase NA

Sponsor

Bolton Medical

36 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02009644

The ClinicalTrials.gov registry entry for NCT02009644 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 158 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bolton Medical, which has 36 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 Abdominal Aortic Aneurysm (AAA) appearing as the primary indexed condition, and to 1 intervention — of which Subjects who receive the Treovance stent-graft 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: NCT02009644 reports 20 study locations spanning 11 distinct geographic areas — top geographies include New York, Illinois, Massachusetts. 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 NCT02009644 about?

NCT02009644 is a clinical study titled "Clinical Study of the Treovance Stent-Graft for Patients With Abdominal Aortic Aneurysms". The purpose of this clinical trial is to assess and evaluate the safety and efficacy of the Treovance Stent-Graft with Navitel Delivery System in subjects with Abdominal Aortic Aneurysms (AAA).

What is the current status of trial NCT02009644?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 158 participants. The study started on 2013-11-23. Estimated completion is 2026-06.

What conditions does trial NCT02009644 study?

This clinical trial studies the following conditions: Abdominal Aortic Aneurysm (AAA). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02009644?

The interventions under investigation include: Subjects who receive the Treovance stent-graft (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02009644?

This trial is sponsored by Bolton Medical, which has 36 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02009644 being conducted?

This trial has 20 study locations across Alabama, Arizona, Connecticut, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial