International Retrospective Study of Pipeline Embolization Device (IntrePED)

Medtronic

Status: Completed

Conditions: Brain Aneurysms

Study type: Observational

Funder types: Industry

Identifiers

NCT01558102

PED001

Details and patient eligibility

About

The primary objective of this retrospective study is to determine the incidence of important safety outcomes in patients who have undergone Pipeline Embolization Device placement for intracranial aneurysms (IAs). This study does not effect patient care, simply it is designed to observe and capture information from numerous hospitals.

Data collection will be initiated starting March 2012 and continue until approximately April 2017.

Enrollment: 793 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• A patient who was treated with the Pipeline Embolization Device for treatment of a brain aneurysm