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Aortic Aneurysm clinical trials

View clinical trials related to Aortic Aneurysm.

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NCT ID: NCT05996354 Active, not recruiting - Aortic Dissection Clinical Trials

Concave Supra-arch Branched Stent-Graft System for Treatment of Aortic Arch Diseases

Start date: March 1, 2022
Phase: N/A
Study type: Interventional

There are no endoluminal stent systems available on the Chinese market for the effective treatment of aortic arch lesions (involving aortic arch aneurysms, aortic coarctation, aortic pseudoaneurysms, aortic ulcers, and intermural hematomas), and therefore this study is intended to be a prospective, single-arm study.

NCT ID: NCT05969782 Active, not recruiting - Aortic Aneurysm Clinical Trials

The Enzen Trial: Comparison of Evar Endoprosthesis: Endurant Versus Zenith

ENZEN
Start date: July 1, 2023
Phase:
Study type: Observational

A prospective, non-randomized trial of patients submitted to EVAR for aortoiliac aneursym using Endurant II (Medtronic) or Zenith (Cook).

NCT ID: NCT05871515 Active, not recruiting - Clinical trials for Abdominal Aortic Aneurysm

3D Ultrasound of Abdominal Aortic Aneurysm Characteristics

3D US - EVAR
Start date: December 27, 2022
Phase:
Study type: Observational

AAA characteristics are traditionally measured with computed tomography angiography (CTA), however, three-dimensional ultrasound (3D US) is emerging as a novel imaging method for AAAs. With the use of a US contrast agent, the AAA thrombus can also be distinguished from the lumen on the 3D scans. This enables 3D visualization of the AAA and its thrombus without the need for harmful radiation and nephrotoxic contrast agents, as opposed to CTA. In in vitro measurements, 3D US has already been shown to have clinically acceptable error rate with AAA diameter and volume measurement. However, it is unclear whether this is also applicable to in vivo measurements. Therefore, the aim of this prospective study is to compare preoperative 3D US AAA characteristics as measured by 3D US with contrast enhancement (3D CEUS), 3D US without contrast enhancement (3D non-CEUS) and CTA.

NCT ID: NCT05650892 Active, not recruiting - Clinical trials for Thoracic Aortic Aneurysm

Male-female Differences in Immunohistological and Biomechanical Properties of the Thoracic Aorta

MAFATS
Start date: February 1, 2021
Phase:
Study type: Observational

Thoracic aortic aneurysms (TAA) result from progressive dilatation of the thoracic aorta and confer a risk for aortic dissection or rupture, which is associated with significant morbidity and mortality. In the Netherlands there are an estimated 200.000 adults with TAA, and annually 600 deaths after aortic dissection or rupture. There are clear differences in the incidence of TAA between men and women, with a higher incidence in men. Little is known on possible differences in outcome between male and female patients with Thoracic Aortic Aneurysm (TAA). Aortic disease is thought to affect men more frequently than women, and aortic growth is different between men and women. Current data suggest that women are at an increased risk of both dying from aortic dissection and having aorta-related complications compared to men (1). The mechanisms for these male-female difference in TAA outcome remain, however, unclear. The timing of preventive surgery is now not different for men and women, but gender-based cut-off values for maximal aortic diameter based on differences in vessel wall composition might be needed.

NCT ID: NCT05421130 Active, not recruiting - Aortic Aneurysm Clinical Trials

Clinical Investigation of Clinical Safety and Performance of the SP-GRIPFLOW, Selective Cerebral Perfusion Catheter When Used for Cerebral Perfusion During Aortic Arch Repair

Start date: May 2, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the SP-GRIPFLOW catheter (the catheter designed by Fuji Systems) is safe and how well it functions. The information from this research will be used to help decide if the device should be approved for sale in the European Union. The SP-GRIPFLOW catheter may not yet be used by investigators outside of the study. Through the study, FUJI will prove that the target flow as measured by the flow through the catheter(s)(cumulative flow for multiple catheters) was confirmed in 95% of cases.

NCT ID: NCT05405790 Active, not recruiting - Aortic Dissection Clinical Trials

Antibiotic Prophylaxis for TEVAR

Start date: January 1, 2022
Phase:
Study type: Observational

The infection rate of thoracic endovascular aortic repair (TEVAR) is unknown due to a lack of epidemiological data. The rate currently available comes from researches conducted decades ago, when open surgery was the standard of care. Because of the potentially fatal consequences of a stent graft infection in the thoracic aorta, the investigators tend to prescribe antibiotic prophylaxis for at least three days. In this study, the investigators are going to collect data on patients receiving TEVAR in the past five years and provide the following information: a. the infection rate (MAGIC classification), b. the rate of fever, c. the results of the lab tests, such as the WBC count and C-reaction protein. d. risk factors associated with infection and fever.

NCT ID: NCT05197543 Active, not recruiting - COVID-19 Clinical Trials

AAA Rupture Risk Assessment in COVID-19 Pandemic

Start date: March 12, 2020
Phase:
Study type: Observational

The acute phase of the COVID-19 pandemic requires a redefinition of healthcare system to increase the number of available intensive care units for COVID-19 patients. This leads to the postponing of elective surgeries including the treatment of abdominal aortic aneurysm (AAA). The probabilistic rupture risk index (PRRI) recently showed its advantage over the diameter criterion in AAA rupture risk assessment. Its major improvement is in increased specificity and yet has the same sensitivity as the maximal diameter criterion. The objective of this study was to test the clinical applicability of the PRRI diagnostic method in a quasi-prospective observational patient cohort study.

NCT ID: NCT05146375 Active, not recruiting - Clinical trials for Thoracic Aortic Aneurysm

Genes Modulating the Severity of Aortic Aneurysms (MSF1-TGFBR2)

MSF1-TGFBR2
Start date: November 24, 2022
Phase:
Study type: Observational

This project concerns a population at risk of sudden death by dissection of the thoracic aorta. Its interest is to make it possible to recognize the genes that protect or worsen the evolution of aneurysms, to better understand the mechanisms involved, to detect and treat aneurysms of the thoracic aorta, wich is a pathology that is completely silent clinically until life-threatening complications. The variability in the severity of the disease within the same family is related to modifier genes. The objective is to find the modifying factors that account for the variability in the severity of the progression of aneurysms of the thoracic aorta.

NCT ID: NCT05133492 Active, not recruiting - Clinical trials for Abdominal Aortic Aneurysm

First In Human Study for Small to Medium-sized Abdominal Aortic Aneurysm (AAA)

AAA
Start date: June 24, 2019
Phase: N/A
Study type: Interventional

This is a first in human study to evaluate the safety and clinical utility of an investigational medical device called the Nectero EAST System to treat Abdominal Aortic Aneurysms or AAA.

NCT ID: NCT05054972 Active, not recruiting - Aortic Aneurysm Clinical Trials

Left Renal Vein Division for Juxtarenal Aortic Exposure

Start date: October 1, 2020
Phase:
Study type: Observational

Retrospective study on the outcome of the renal function in patients operated because of juxtarenal aortic aneurysms.