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Popliteal Artery Aneurysm clinical trials

View clinical trials related to Popliteal Artery Aneurysm.

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NCT ID: NCT05360108 Recruiting - Clinical trials for Aortic Aneurysm, Abdominal

Screening for Abdominal Aortic Aneurysm and Popliteal Artery Aneurysm

DAAP-PR
Start date: June 1, 2020
Phase:
Study type: Observational

Observational, prospective, cohort study to evaluate, by an opportunistic screening program based on vascular ultrasound, the prevalence and characteristics of Abdominal Aortic Aneurysm (AAA) and Popliteal Artery Aneurysm (PAA) in a female population as well as the prevalence and characteristics of PAA in male population.

NCT ID: NCT04907240 Recruiting - Clinical trials for Peripheral Artery Disease

Observational GORE® VIABAHN® Endoprosthesis With PROPATEN Bioactive Surface Global Registry

Start date: October 9, 2021
Phase:
Study type: Observational [Patient Registry]

Collect real-world post-market clinical follow-up data on patients treated with the GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface (VSX)

NCT ID: NCT04188808 Recruiting - Quality of Life Clinical Trials

Prospective Case-control Study in Patients With PAA

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

The overall objective is to highlight different aspects of care in patients with PAA before and after treatment, and identifying factors that influence the outcome of PAA patients.

NCT ID: NCT02867501 Completed - Vascular Diseases Clinical Trials

Venous Distension in Patients With Aneurysmatic Arterial Disease

Start date: May 2016
Phase: N/A
Study type: Observational

The aim of the study is to assess if venous distension in patients with aneurysmatic arteriopathy is higher compared to patients with peripheral arterial occlusive disease (PAOD) and in controls.

NCT ID: NCT02462876 Completed - Clinical trials for Popliteal Artery Aneurysm

Evaluation of the GORE® VIABAHN® Endoprosthesis for the Treatment of Popliteal Artery Aneurysm (PAA)

Start date: October 2015
Phase:
Study type: Observational

This study will assess the long term safety and performance of the GORE® VIABAHN® Endoprosthesis for the treatment of patients with Popliteal Artery Aneurysms.

NCT ID: NCT01902888 Terminated - Clinical trials for Popliteal Artery Aneurysm

Evaluation of GORE® VIABAHN® Endoprosthesis for Popliteal Artery Aneurysm

PAA 12-01
Start date: July 2013
Phase: N/A
Study type: Observational

This is a multicenter, non-randomized, single arm, retrospective study of GORE® VIABAHN® Endoprosthesis for the treatment of a Popliteal Artery Aneurysm (PAA).

NCT ID: NCT01817660 Terminated - Clinical trials for Popliteal Artery Aneurysm

Open Versus Endovascular Repair of Popliteal Artery Aneurysm Trial

OVERPAR
Start date: February 2013
Phase: N/A
Study type: Interventional

Weakness in the wall of a blood vessel located behind the knee (popliteal artery) which leads to a swelling of this blood vessel (aneurysm) is one of the most common types of arterial aneurysms. It is associated with significant risk of blood clot formation, narrowing of blood vessel which can create a serious threat to individual's health. Currently, approved treatment options for this condition include both open surgical and endovascular stent-graft repairs. In the open repair procedure, the blood vessel behind the knee is tied up or removed and a small artery is created using a vein on the same leg. This is also called a bypass procedure. In the endovascular repair, using X-rays, doctors places a stent in the blood vessel. Stent is a small device similar to a thin tube. When it is placed in the right location, your doctor can open it. When stent is opened, it supports weakened blood vessel and blood goes through it. The weakened artery then shrinks around the stent. The OVER-PAR is a short name for this study. Many hospitals in the United States agreed to participate in this study. Patients are randomized to undergo either open or endovascular repair because they can be treated with either of the procedures. Investigators use the short names OPAR for open surgical repair and EPAR for endovascular repair. People who have an aneurysm that is larger than 2 cm (about an inch) can participate in this study. The purpose of this study is to compare outcomes after these two standard procedures.