Outcome Study of the Pipeline Embolization Device With Vantage Technology in Unruptured Aneurysms

N/AActive Not RecruitingNCT05626504

King's College Hospital NHS Trust50 enrolled

Overview

In this project the investigators study the safety and efficacy of the pipeline embolization device with vantage technology in treatment of unruptured brain aneurysms

Study Type

OBSERVATIONAL

Enrollment

Conditions

Brain Aneurysm Intracranial Hemorrhages Stroke

Interventions

Pipeline Embolization Device with Vantage TechnologyDEVICE

Flow-diverter device occludes aneurysms through endoluminal reconstruction and remodelling of the parent artery.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * All patients treated with Pipeline Embolization Device with Vantage Technology (PEDV) * MRA and/or DSA (or tomographic angiography) available for follow up Exclusion Criteria: * Insufficient background data available e.g., to determine size of aneurysm and pipeline device * PEDV used for causes other than aneurysms, e.g., fistulas and dissection.

Locations (1)

Kings College Hospital

London, United Kingdom

Outcomes

Primary Outcomes

Evaluate 30-day morbidity rates

We will evaluate short term clinical outcome in the form of morbidity rates 30 days after the procedure

Time frame: Done at 30 days post procedural

Evaluate 30-day mortality rates

We will evaluate short term clinical outcome in the form of mortality rates 30 days after the procedure

Time frame: Done at 30 days post procedural

Secondary Outcomes

Evaluate 1-year morbidity rates

We will evaluate long term clinical outcome in the form of morbidity rates \>30days up to 1 year after the procedure

Time frame: Done at >30days up to 1 year post procedural

Evaluate 1-year mortality rates

We will evaluate long term clinical outcome in the form of mortality rates \>30days up to 1 year after the procedure

Time frame: Done at >30days up to 1 year post procedural

Data from ClinicalTrials.gov

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