Clinical trials: Abdominal Aortic
Hemodynamic Instability
Hemodynamic Monitoring During Abdominal Aortic Surgery
This trial investigates the ability of our istitutional algorithm in maintaining a safe hemodynamics during abdominal aorta open surgery, in terms of limitation of intraoperative hypotension incidence
- Trial name
- HEMAS (NCT05478564)
- Testing
- Intraoperative fluids and vasoactive drugs management protocol
- Where
- Italy
- Volunteers
- 63 people
- Sponsor
- Humanitas Clinical and Research Center
Abdominal Aortic Aneurysm, Aorto-iliac Aneurysm
Zenith® LP Abdominal Aortic Aneurysm (AAA) Post-Market Registry
A registry to collect additional prospective intra-operative and follow-up information on physician use of the CE-marked Zenith® Low Profile Abdominal Aortic Aneurysm (AAA) Endovascular Graft under routine clinical care.
- Trial name
- NCT01424267
- Testing
- Zenith® Low Profile AAA Endovascular Graft
- Where
- 15 sites in Austria, Germany and 5 more
- Volunteers
- 76 people
- Sponsor
- Cook Group Incorporated
Aortic Aneurysm, Thoracoabdominal, Aortic Aneurysm, Thoracic
Endovascular Treatment of TAAA and Aortic Arch Aneurysms Using Fenestrated and Branched Stent Grafts
Prospective, nonrandomized, single-center, two-arm study to assess the feasibility and safety and to evaluate clinical outcomes of endovascular repair of complex aortic aneurysms (thoracoabdominal aortic aneurysms and aortic arch…
- Conditions
- Aortic Aneurysm, Thoracoabdominal, Aortic Aneurysm, Thoracic, Aortic Dissection, Thoracoabdominal
- Trial name
- NCT02323581
- Testing
- Endovascular treatment of Thoracoabdominal Aortic Aneurysm, Endovascular treatment of Aortic Arch Aneurysms
- Where
- 2 sites in United States
- Volunteers
- 520 people
- Sponsor
- Darren Schneider, M.D.
Abdominal Aneurysm, Endovascular Aortic Repair
Pre-emptive Coil Embolization in Endovascular Aortic Repair
Abdominal aortic aneurysms are often treated with a minimally invasive procedure called endovascular aortic repair (EVAR). While EVAR is widely used, it can sometimes lead to complications over time, and some patients may require…
- Conditions
- Abdominal Aneurysm, Endovascular Aortic Repair, Endoleak
- Trial name
- PRIZE (NCT06975215)
- Testing
- Concomitant embolization, EVAR
- Volunteers
- 332 people
- Sponsor
- Uppsala University
Vascular Disease
Efficacy of Patient Centred Information for Vascular Disease
This study aims to determine the usefulness of providing patients with web-based electronically accessed patient information when compared to the provision of written information leaflets.
- Trial name
- NCT01804972
- Testing
- Verbal and written information, Verbal and electronic information
- Where
- Ireland
- Volunteers
- 50 people
- Sponsor
- Mid Western Regional Hospital, Ireland
Aneurysm Abdominal, Endovacular Repair
Post Implantation Syndrome and Administration on NSAIDs in Patients Undergoing EVAR for AAA
INTRODUCTION Post-implantation syndrome is the clinical and biochemical expression of an inflammatory response following endovascular repair of an aortic aneurysm.
- Trial name
- NCT03727412
- Testing
- Drugs, Generic (Naprosyn)
- Where
- Greece
- Volunteers
- 186 people
- Sponsor
- University of Thessaly
Abdominal Aortic Aneurysm
GORE® EXCLUDER® Endoprosthesis French Mandatory Registry
This is a French Registry mandated by the French National Health Authority assessing long-term (5-years) safety of the GORE® Excluder® Endoprosthesis in the treatment of infra-renal Abdominal Aortic Aneurysms (AAA).
- Trial name
- NCT02308839
- Testing
- GORE® EXCLUDER® Endoprosthesis
- Where
- France
- Volunteers
- 181 people
- Sponsor
- W.L.Gore & Associates
Abdominal Aortic Aneurysm, AAA
Screening Cardiovascular Patients for Aortic aNeurysms (SCAN)
The aim of the cohort study SCAN (Screening Cardiovascular patients for Aortic aNeurysms) is to establish a screening programm for patients with a high risk for an AAA.
- Trial name
- SCAN (NCT02179801)
- Where
- 2 sites in Germany
- Volunteers
- 1,000 people
- Sponsor
- Technical University of Munich
Blood Transfusion
Allogenic Blood Transfusion During Elective Open Abdominal Aortic Surgery
Open surgery on the abdominal aorta is a high risk procedure associated with an intravascular volume blood loss and thereby, with high requirement for blood and blood product transfusion.
- Trial name
- NCT03891303
- Testing
- Allogenic blood transfusion (ABT)
- Volunteers
- 426 people
- Sponsor
- Clinic for Cardiovascular Diseases Magdalena
Aortic Aneurysm, Abdominal
Non Invasive Imaging of Abdominal Aorta Aneurysm Hemodynamics and Wall Structure
The development of the abdominal aorta aneurysm is multifactorial. Through use of magnetic resonance imaging without contrast, this study will look closely at flow, the stresses hereby induced, as well as signs of inflammation in…
- Trial name
- NCT01104688
- Where
- Denmark
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Aarhus University Hospital
Thoracoabdominal Aortic Aneurysm, Without Mention of Rupture, Abdominal Aortic Aneurysm Without Rupture
Shockwave™Peripheral Intravascular Lithotripsy Balloon for Advanced Endovascular Aortic Repair
Shockwave TEVAR is a nonrandomized, prospective, international, multi-center, PMCF, obervational study. The aim of this study is to evaluate the outcomes of the Shockwave™ Peripheral Intravascular Lithotripsy Balloon (Shockwave…
- Conditions
- Thoracoabdominal Aortic Aneurysm, Without Mention of Rupture, Abdominal Aortic Aneurysm Without Rupture, Thoracic Aortic Aneurysm Without Rupture
- Trial name
- TEVAR (NCT06332911)
- Testing
- Shockwave™ Peripheral Intravascular Lithotripsy Balloon M5+
- Where
- 5 sites in Germany, Italy and 1 more
- Volunteers
- 30 people
- Sponsor
- Rede Optimus Hospitalar SA
Aortic Aneurysm Abdominal
Zenith® p-Branch® Endovascular Graft Pivotal Study
The Zenith® p-Branch® Pivotal Study is a clinical trial approved by FDA to study the safety and effectiveness of the Zenith® p-Branch® endovascular graft in combination with the Atrium iCAST™ covered stents in the treatment of…
- Trial name
- NCT02396199
- Testing
- Zenith® p-Branch® in combination with the Atrium iCAST™ covered stents
- Where
- 27 sites in United States
- Volunteers
- 80 people
- Sponsor
- Cook Research Incorporated
Abdominal Aortic Aneurysm
Suprarenal Proximal Cuff Study for Treatment of Abdominal Aortic Aneurysm
The use of a suprarenal extension device during the index AAA procedure to accommodate the patient's anatomy and to prevent or repair leakage.
- Trial name
- NCT00739401
- Testing
- Suprarenal Proximal Cuff Extension
- Where
- 8 sites in United States
- Volunteers
- 44 people
- Sponsor
- Endologix
Aortic Aneurysm, Abdominal, Pain
Efficacy of the Ultrasound-guided Transversus Abdominis Plane Block in Open Aortic Abdominal Aneurysm Repair Surgery
The ETAP study aim to assess the effect of the addition of an ultrasound-guided transversus abdominis plane (TAP) block to a multimodal intravenous analgesia protocol on the postoperative pain control in open surgical repair of…
- Conditions
- Aortic Aneurysm, Abdominal, Pain, Anesthesia, Local
- Trial name
- ETAP (NCT02292667)
- Testing
- TAP block, PCA with Chlorhydrate of Morphine, Acetaminophen
- Where
- France
- Volunteers
- 60 people
- Sponsor
- Centre Hospitalier Universitaire de Besancon
Abdominal Aortic Aneurysm, Abdominal Aortic Stenosis
Effectiveness of TAP (Transversus Abdominis Plane) Block for Abdominal Aortic Surgery
The goal of this study is to learn about the effectiveness of TAP block for pain relief after vascular surgery on the abdominal aorta.
- Conditions
- Abdominal Aortic Aneurysm, Abdominal Aortic Stenosis, Syndrome, Leriche
- Trial name
- NCT05860452
- Testing
- ropivacaine, normal saline
- Where
- Slovenia
- Volunteers
- 30 people
- Sponsor
- University Medical Centre Ljubljana
Abdominal Aorta Aneurysm
Performance and Safety of a Second Generation Antimicrobial Graft in Abdominal Position
Safety and performance of an anti-microbial vascular graft in the treatment of aneurysmal and occlusive disease of the abdominal aorta.
- Trial name
- SYNERGY (NCT01710878)
- Testing
- Intergard Synergy Graft
- Where
- 8 sites in France, Germany
- Volunteers
- 60 people
- Sponsor
- Maquet Cardiovascular
Hemorrhage
POCUS-PEAC to Reduce Femoral Arterial Blood Flow
The aim of this study is to evaluate the efficacy on healthy subjects of Point of Care ultrasonographically guided external aortic compression compared to the manual technique already described.
- Trial name
- NCT04745585
- Where
- Canada
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
Aneurysm, Abdominal Aortic
Interest of a Post-operative Ultrasound With Systematic Use of Ultrasonic Contrast in the Follow-up of Aortic Endoprosthesis: Prospective Study at the University Hospital of Nice
This is a prospective study conducted on a population with an aortic endoprosthesis in the context of an abdominal aortic aneurysm.
- Trial name
- Ultra_Evar (NCT04196543)
- Testing
- écho-doppler with ultrasonar Sonovue® injection
- Where
- France
- Volunteers
- 40 people
- Sponsor
- Centre Hospitalier Universitaire de Nice
Abdominal Aortic Aneurysm, Peripheral Artery Disease
A Study of Remote Ischaemic Preconditioning in Patients With Atherosclerosis Undergoing Vascular Surgery
The purpose of this study is to evaluate the effect of preoperative remote ischaemic preconditioning (RIPC) on organ damage and the functional characteristics of arteries in patients undergoing vascular surgery.
- Conditions
- Abdominal Aortic Aneurysm, Peripheral Artery Disease, Carotid Artery Stenosis
- Trial name
- NCT02689414
- Testing
- Remote ischaemic preconditioning, Control to RIPC
- Where
- Estonia
- Volunteers
- 98 people
- Sponsor
- Tartu University Hospital
Abdominal Aortic Aneurysm, Abdominal Aortic Aneurysm Enlargement
Italian Multicenter Database for Open Conversions After EVAR
Late endovascular abdominal aneurysm repair (EVAR) complications not amenable to endovascular correction can undergo either late open conversion (LOC) or semi-conversion (SC).
- Trial name
- iConveRt (NCT04299984)
- Testing
- Open Conversion after EVAR, SemiConversion after EVAR
- Where
- Italy
- Volunteers
- 500 people
- Sponsor
- Azienda Ospedaliero-Universitaria di Parma