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NCT02998229 · ClinicalTrials.gov registry record · NA

The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck Bifurcating Intracranial Aneurysms (IAs).

A NA study of Intracranial Aneurysm, sponsored by Medtronic Neurovascular Clinical Affairs.

Recruiting
Registry status
NA
Development phase
300
Enrollment target
19
Study locations

NCT02998229: Recruiting NA study of Intracranial Aneurysm, sponsored by Medtronic Neurovascular Clinical Affairs.

NCT02998229 is a NA study of Intracranial Aneurysm that is actively recruiting participants, run by Medtronic Neurovascular Clinical Affairs. The registered enrollment target is 300 participants, below the 9,175-participant average among 14 other Intracranial Aneurysm trials with a reported enrollment target (97% lower). The trial reports 19 study locations across 12 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02998229, a NA study of Intracranial Aneurysm, is actively recruiting participants, sponsored by Medtronic Neurovascular Clinical Affairs.

RECRUITING
Registry status
NA
Development phase
300 participants
Enrollment target
19
Study locations

Study Summary

The purpose of this study is to assess the safety and effectiveness of the Artisse™ Intrasaccular Device in the treatment of unruptured and ruptured wide-neck bifurcating intracranial aneurysms.

Primary Outcome

Incidence of complete aneurysm occlusion without retreatment of the target aneurysm, recurrent subarachnoid hemorrhage (SAH) from the target aneurysm, or significant parent artery stenosis (\>50% stenosis) at 1 year post-procedure.

Conditions Studied

Interventions

  • DEVICE Artisse™ Intrasaccular Device

Study Locations (19)

New York

  • Albany Medical Center - Albany
  • Buffalo General Medical Center - Buffalo
  • The Mount Sinai Hospital - New York
  • Stony Brook University Hospital - Stony Brook

Pennsylvania

  • Hospital of the University of Pennsylvania - Philadelphia
  • Thomas Jefferson University Hospital - Philadelphia
  • UPMC Presbyterian - Pittsburgh

Florida

  • Baptist Medical Center Jacksonville - Jacksonville
  • Tampa General Hospital - Tampa

Illinois

  • University of Chicago - Chicago
  • Advocate Lutheran General Hospital - Park Ridge

Connecticut

  • Yale New Haven Hospital - New Haven

Iowa

  • University of Iowa Hospitals and Clinics - Iowa City

North Carolina

  • Novant Health Brain and Spine Surgery - Charlotte

Ohio

  • Cleveland Clinic Foundation - Cleveland

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2024-04-16
Est. Completion 2032-02
Phase NA

What NCT02998229 shows while recruiting

NCT02998229 is an interventional study that assigns participants to a tested intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, below the 9,175-participant average among 14 other Intracranial Aneurysm trials with a reported enrollment target (97% lower).

The record links to 1 condition, with Intracranial Aneurysm appearing as the primary indexed condition, and to 1 intervention - of which Artisse™ Intrasaccular Device is the first listed.

NCT02998229 lists 19 locations in 12 states (New York, Pennsylvania, Florida).

Frequently Asked Questions

What is clinical trial NCT02998229 about?

NCT02998229 is a clinical study titled "The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck Bifurcating Intracranial Aneurysms (IAs).". The purpose of this study is to assess the safety and effectiveness of the Artisse™ Intrasaccular Device in the treatment of unruptured and ruptured wide-neck bifurcating intracranial aneurysms.

What is the current status of trial NCT02998229?

This trial is currently recruiting. It is a NA study. The enrollment target is 300 participants. The study started on 2024-04-16. Estimated completion is 2032-02.

What conditions does trial NCT02998229 study?

This clinical trial studies the following conditions: Intracranial Aneurysm.

What interventions are being tested in trial NCT02998229?

The interventions under investigation include: Artisse™ Intrasaccular Device (DEVICE).

Who is sponsoring clinical trial NCT02998229?

This trial is sponsored by Medtronic Neurovascular Clinical Affairs, which has 20 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02998229 being conducted?

This trial has 19 study locations across Connecticut, Florida, Illinois, Iowa, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Intracranial Aneurysm

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02998229's enrollment target sits among peer trials

300 7th of 14 higher than 8 of 14 other Intracranial Aneurysm trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Intracranial Aneurysm trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02998229, the US trial registry maintained by the National Library of Medicine. NCT02998229 (mid enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.