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Abdominal Aortic Aneurysm (AAA) clinical trials

View clinical trials related to Abdominal Aortic Aneurysm (AAA).

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NCT ID: NCT04592991 Terminated - Clinical trials for Abdominal Aortic Aneurysm (AAA)

CCR2 AAA Pilot Study

Start date: October 7, 2020
Phase: Early Phase 1
Study type: Interventional

The purpose of this research study is to look at whether an investigational imaging agent, 64Cu-DOTA-ECL1i, used during Positron Emission Tomography (PET)/ Computed Tomography (CT) scanning, can help to identify conditions that place patients at an increased risk for AAA rupture. The study is also looking more closely at cellular, molecular and inflammatory properties of the aortic wall. Having the ability to identify markers that predict AAA progression/expansion and risk for rupture could allow the physician to manage patients in a more individualized, personal way.

NCT ID: NCT03231397 Terminated - Clinical trials for Abdominal Aortic Aneurysm (AAA)

Predictors of AAA Expansion and/or Rupture

Start date: August 1, 2017
Phase: Phase 4
Study type: Interventional

Eligible subjects in this study will have either a known abdominal aortic aneurysm (AAA) or because they do not have an AAA (control group). The purpose of this research study is to further study, through FEA, changes that occur in the mechanical properties of the aortic wall. The investigator will compare two radiotracers, 18F-FDG and 11C-PBR28 to determine if one provides more useful and reliable information about inflammation. 18F-FDG and 11C-PBR28 are radioactive drugs that will be used for imaging during the PET-CT scan. The investigator will also compare the results describing the mechanical properties of the AAA wall to the degree of inflammation in that wall as determined by PET-CT imaging to define new and better predictors of AAA growth and/or rupture.

NCT ID: NCT02007252 Terminated - Clinical trials for Abdominal Aortic Aneurysm (AAA)

ACZ885 for the Treatment of Abdominal Aortic Aneurysm

AAA
Start date: December 2013
Phase: Phase 2
Study type: Interventional

This study was designed to assess the safety, tolerability and efficacy of ACZ885 on aneurysmal growth rate in subjects with abdominal aortic aneurysms (AAA). The purpose of the study was to provide data to enable decisions regarding the further development of ACZ885 for subjects with abdominal aortic aneurysms. The design of this study addressed the primary objective of evaluating the change in aneurysmal size in subjects with AAA as a result of treatment with ACZ885.