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RECRUITING NA

Safety and Efficacy of Endovascular Treatment of Intracranial Aneurysms With Surpass Elite With GUARDian Flow Diverter (GUARD)

NCT06872684 · View on ClinicalTrials.gov ↗

Study Summary

The objective of the Safety and Efficacy of Endovascular Treatment of Intracranial Aneurysms with Surpass Elite with GUARDian Flow Diverter (GUARD) trial is to evaluate the safety and efficacy of the Surpass Elite with Guardian Flow Diverter System (FDS) in the treatment of unruptured, wide-neck saccular or fusiform, intracranial aneurysms (IAs) located on the internal carotid artery (ICA) or its branches.

Interventions

  • DEVICE Surpass Elite with Guardian Flow Diverter System

Study Locations (3)

Arizona

  • Carondelet St. Joseph's Hospital — Tucson

California

  • University of California Davis Health — Davis

Massachusetts

  • Lahey Hospital and Medical Center — Burlington

Trial Details

FieldValue
Enrollment Target 183 participants
Start Date 2025-06-20
Est. Completion 2031-01-31
Phase NA

Sponsor

Stryker Neurovascular

5 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06872684

The ClinicalTrials.gov registry entry for NCT06872684 describes a study currently listed as 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 183 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 2 conditions, with Aneurysm appearing as the primary indexed condition, and to 1 intervention — of which Surpass Elite with Guardian Flow Diverter 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: NCT06872684 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Arizona, California, 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 NCT06872684 about?

NCT06872684 is a clinical study titled "Safety and Efficacy of Endovascular Treatment of Intracranial Aneurysms With Surpass Elite With GUARDian Flow Diverter (GUARD)". The objective of the Safety and Efficacy of Endovascular Treatment of Intracranial Aneurysms with Surpass Elite with GUARDian Flow Diverter (GUARD) trial is to evaluate the safety and efficacy of the Surpass Elite with Guardian Flow Diverter System (FDS) in the treatment of unruptured, wide-neck sac...

What is the current status of trial NCT06872684?

This trial is currently recruiting. It is a NA study. The enrollment target is 183 participants. The study started on 2025-06-20. Estimated completion is 2031-01-31.

What conditions does trial NCT06872684 study?

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

What interventions are being tested in trial NCT06872684?

The interventions under investigation include: Surpass Elite with Guardian Flow Diverter System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06872684?

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 NCT06872684 being conducted?

This trial has 3 study locations across Arizona, California, Massachusetts. 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