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Aneurysm clinical trials

View clinical trials related to Aneurysm.

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NCT ID: NCT04315168 Completed - Clinical trials for Intracranial Aneurysm

FRED and FRED JR Devices for Intracranial Aneurysm Treatment

Start date: June 12, 2020
Phase:
Study type: Observational [Patient Registry]

A French, multicenter, prospective, observational, "real-world" assessment of the safety and efficacy of FRED and FRED Jr devices in the treatment of intracranial aneurysms

NCT ID: NCT04307888 Not yet recruiting - Clinical trials for Aortic Valve Stenosis

Spanish Percutaneous Aortic INtervention REGISTRY (SPAIN REGISTRY)

SPAIN
Start date: April 2020
Phase:
Study type: Observational [Patient Registry]

Multicentre prospective registry including consecutive patients undergoing Percutaneous Endovascular Aneurysm Repair (PEVAR), Percutaneous Endovascular Thoracic Aneurysm Repair (PTEVAR) or Transcatheter Aortic Valve Implantation (TAVI) in which variables related to the percutaneous access closure for implanting devices at aorta level will be collected and analyzed. The follow-up period will be 30 days after the procedure. The duration of the recruitment period will be one year. All data will be collected telematically and incorporated into a database for subsequent statistical analysis. There will be 2 points for data interim analysis at 6 and 12 months after initiation of the study.

NCT ID: NCT04305704 Recruiting - Vascular Diseases Clinical Trials

Coated Mongolian Aneurysm Treatment Study 2

COMATS 2
Start date: February 8, 2020
Phase:
Study type: Observational

The purpose of this study is to assess safety and effectiveness of the p64 MW HPC or p48 MW HPC Flow Modulation Device under prasugrel.

NCT ID: NCT04305626 Recruiting - Vascular Diseases Clinical Trials

Coated Mongolian Aneurysm Treatment Study 1

COMATS 1
Start date: June 22, 2019
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to assess safety and effectiveness of the p64 MW HPC or p48 MW HPC Flow Modulation Device under Dual Antiplatelet Medication.

NCT ID: NCT04299984 Not yet recruiting - Clinical trials for Abdominal Aortic Aneurysm

Italian Multicenter Database for Open Conversions After EVAR

iConveRt
Start date: August 1, 2020
Phase:
Study type: Observational [Patient Registry]

Late endovascular abdominal aneurysm repair (EVAR) complications not amenable to endovascular correction can undergo either late open conversion (LOC) or semi-conversion (SC). LOC is defined as a total or partial endograft explantation >30 days after the initial EVAR. SC is defined as open or laparoscopic surgery for endoleak (EL) correction with complete endograft preservation. The aim of this study is to collect in a prospective database the technical aspects of a multicenter experience of LOC and SC, and to analyse early and long-term outcomes of these two treatments.

NCT ID: NCT04292652 Recruiting - Clinical trials for Aortic Aneurysm, Abdominal

Myocardial Injury in Treatment of AAA

TREATROP
Start date: January 1, 2007
Phase:
Study type: Observational

Comparison of elective infrarenal aneurysm surgery with open and endovascular technique, respectively, for subclinical ischemic myocardial injury detectable with troponin T and/or 3-channel Holter ECG with ST analysis

NCT ID: NCT04289480 Active, not recruiting - Clinical trials for Intracranial Aneurysm

Safety and Effectiveness of ENTERPRISE 2 Device in the Endovascular Treatment of Intracranial Aneurysms

EMPOWER
Start date: July 30, 2020
Phase:
Study type: Observational

The study is designed to evaluate the safety and effectiveness of ENTERPRISE 2 vascular reconstruction device and delivery system (hereinafter referred to as ENTERPRISE 2) to facilitate endovascular coil embolization of intracranial aneurysms.

NCT ID: NCT04269447 Enrolling by invitation - Aortic Aneurysm Clinical Trials

Prospective Aortic Biobank of POP-STAR

Start date: November 18, 2019
Phase:
Study type: Observational [Patient Registry]

The overall objective of the POP-STAR project is individualized surveillance for patients diagnosed with abdominal aortic aneurysms by means of more precise, patient-specific AAA growth prediction.

NCT ID: NCT04269408 Completed - Clinical trials for Aneurysmal Subarachnoid Hemorrhage

A Safety and Efficacy Study of NicaPlant® in Aneurysmal Subarachnoid Haemorrhage Patients Undergoing Aneurysm Clipping

Start date: April 5, 2020
Phase: Phase 2
Study type: Interventional

This study of NicaPlant® is conducted in patients who have a subarachnoid haemorrhage. Patients will be randomized in two treatment groups. Both groups will receive the standard of care and the investigational group will receive in addition NicaPlant®. NicaPlant® is tested to reduce the long-term complications of aneurysmal subarachnoid haemorrhage (aSAH).

NCT ID: NCT04252573 Active, not recruiting - Clinical trials for 2 Juxtarenal Abdominal Aortic Aneurysm

Chimney EndoVascular Aneurysm Sealing Of New Expanded Indication

ChEVAS One
Start date: June 29, 2020
Phase: N/A
Study type: Interventional

Prospective, multi-center, non-randomized study with consecutive, eligible subject enrollment at each site, for the evaluation of the ChEVAS System for Endovascular Repair of Complex Abdominal Aortic Aneurysms.