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NCT06872684 · ClinicalTrials.gov registry record · NA

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

A NA study of Aneurysm and Aneurysm, Intracranial, sponsored by Stryker Neurovascular.

Recruiting
Registry status
NA
Development phase
183
Enrollment target
3
Study locations

NCT06872684 is a NA study of Aneurysm and Aneurysm, Intracranial that is actively recruiting participants, run by Stryker Neurovascular. The registered enrollment target is 183 participants, below the 17,066-participant average among 6 other Aneurysm trials with a reported enrollment target (99% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT06872684, a NA study of Aneurysm and Aneurysm, Intracranial, is actively recruiting participants, sponsored by Stryker Neurovascular.

RECRUITING
Registry status
NA
Development phase
183 participants
Enrollment target
3
Study locations

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

13 total trials

What the Registry Record Tells You About NCT06872684

The ClinicalTrials.gov registry entry for NCT06872684 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 183 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 17,066-participant average among 6 other Aneurysm trials with a reported enrollment target (99% lower). The listed sponsor is Stryker Neurovascular, which has 13 total studies on file at ClinicalTrials.gov.

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.

NCT06872684 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Arizona, California, Massachusetts.

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.

What interventions are being tested in trial NCT06872684?

The interventions under investigation include: Surpass Elite with Guardian Flow Diverter System (DEVICE).

Who is sponsoring clinical trial NCT06872684?

This trial is sponsored by Stryker Neurovascular, which has 13 total clinical trials registered on ClinicalTrials.gov.

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.

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

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