Stroke Clinical Trial
— PEDVUOfficial title:
Outcome Study of the Pipeline Embolization Device With Vantage Technology in Unruptured Aneurysms
Verified date | March 2024 |
Source | King's College Hospital NHS Trust |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
In this project the investigators study the safety and efficacy of the pipeline embolization device with vantage technology in treatment of unruptured brain aneurysms
Status | Active, not recruiting |
Enrollment | 50 |
Est. completion date | March 31, 2025 |
Est. primary completion date | March 1, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Kings College Hospital | London |
Lead Sponsor | Collaborator |
---|---|
King's College Hospital NHS Trust |
United Kingdom,
Atasoy D, Kandasamy N, Hart J, Lynch J, Yang SH, Walsh D, Tolias C, Booth TC. Outcome Study of the Pipeline Embolization Device with Shield Technology in Unruptured Aneurysms (PEDSU). AJNR Am J Neuroradiol. 2019 Dec;40(12):2094-2101. doi: 10.3174/ajnr.A6314. Epub 2019 Nov 14. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evaluate 30-day morbidity rates | We will evaluate short term clinical outcome in the form of morbidity rates 30 days after the procedure | Done at 30 days post procedural | |
Primary | Evaluate 30-day mortality rates | We will evaluate short term clinical outcome in the form of mortality rates 30 days after the procedure | Done at 30 days post procedural | |
Secondary | 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 | Done at >30days up to 1 year post procedural | |
Secondary | 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 | Done at >30days up to 1 year post procedural |
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