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

B

Balt

Status

Completed

Conditions

Intracranial Aneurysm

Treatments

Device: LEO +

Study type

Observational

Funder types

Industry

Identifiers

NCT03504436
LEO + II

Details and patient eligibility

About

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.

Enrollment

176 patients

Sex

All

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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