CompletedNot Applicable

Endovascular Treatment of Wide Neck Intracranial Aneurysms With the LEO + Stent : The LEO + II Cohort Study

176 participantsStarted 2015-03-15

Plain-language summary

This is a prospective, multicenter, single-arm observational study to evaluate the efficacy and the morbi-mortality of LEO + in patients with wide neck intracranial aneurysms (fusiform, saccular or dissecting), ruptured or not ruptured.

Who can participate

SexALL

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Inclusion Criteria: * All patients with ruptured or not ruptured intracranial aneurysms demonstrated by cerebral arteriography treated with LEO + stent * Patients (or their parents for minors) must be informed and give written consent Exclusion Criteria: * Patients (or parents) who refused to give consent.

What they're measuring

Total aneurysmal occlusion rate

Timeframe: 18 months

Morbi-mortality

Timeframe: 18 months

Trial details

NCT IDNCT03504436

SponsorBalt Extrusion

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2019-01-07

View on ClinicalTrials.gov More Intracranial Aneurysm trials