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NCT06872684: GUARD

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

Recruiting now NA Last updated 8 April 2026
What this trial tests

NA trial testing Surpass Elite with Guardian Flow Diverter System in Aneurysm in 183 participants. Currently enrolling.

Timeline
20 June 2025
Primary endpoint
31 January 2029
31 January 2031

Quick facts

Lead sponsorStryker Neurovascular
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment183
Start date20 June 2025
Primary completion31 January 2029
Estimated completion31 January 2031
Sites10 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Stryker Neurovascular — full company profile →

Who can join

Adults 18 to 80, any sex, with Aneurysm or Aneurysm, Intracranial. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Aneurysm

Currently open trials in the same condition.

Other Stryker Neurovascular trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06872684.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing