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COMPLETED NA

Neuroform Atlas Stent System Study

NCT02340585 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to demonstrate effectiveness and safety of the Neuroform Atlas Stent System for use with bare metal embolic coils.

Conditions Studied

Interventions

  • DEVICE Next Generation Neuroform Stent System

Study Locations (20)

Massachusetts

  • Tufts Medical Center — Boston
  • Beth Israel Deaconess Medical Center — Boston
  • University of Massachusetts Medical School — Worcester

California

  • Cedars-Sinai Medical Center — Los Angeles
  • Vascular Neurology of Southern California — Thousand Oaks

Ohio

  • The Cleveland Clinic Foundation — Cleveland
  • Mercy Health - St. Vincent Medical Center — Toledo

Pennsylvania

  • Hospital of the University of Pennsylvania — Philadelphia
  • University of Pittsburgh Medical Center — Pittsburgh

Colorado

  • Radiology Imaging Associates — Englewood

Delaware

  • Christiana Care Health Services — Newark

Florida

  • Lyerly Neurosurgery — Jacksonville

Georgia

  • WellStar Kennestone Hospital — Marietta

Trial Details

FieldValue
Enrollment Target 298 participants
Start Date 2015-06-18
Est. Completion 2022-09-30
Phase NA

Sponsor

Stryker Neurovascular

5 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02340585

The ClinicalTrials.gov registry entry for NCT02340585 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 298 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stryker Neurovascular, which has 5 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 Intracranial Aneurysm appearing as the primary indexed condition, and to 1 intervention — of which Next Generation Neuroform Stent 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: NCT02340585 reports 20 study locations spanning 15 distinct geographic areas — top geographies include Massachusetts, California, Ohio. 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 NCT02340585 about?

NCT02340585 is a clinical study titled "Neuroform Atlas Stent System Study". The primary objective of this study is to demonstrate effectiveness and safety of the Neuroform Atlas Stent System for use with bare metal embolic coils.

What is the current status of trial NCT02340585?

This trial is currently completed. It is a NA study. The enrollment target is 298 participants. The study started on 2015-06-18. Estimated completion is 2022-09-30.

What conditions does trial NCT02340585 study?

This clinical trial studies the following conditions: Intracranial Aneurysm. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02340585?

The interventions under investigation include: Next Generation Neuroform Stent System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02340585?

This trial is sponsored by Stryker Neurovascular, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02340585 being conducted?

This trial has 20 study locations across California, Colorado, Delaware, 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