Aneurysms Aortic Arch Clinical Trial
— FETOPTOfficial title:
Evaluation of Supra-aortic Trunks Debranching Techniques in Open Arch Repair by Means of Frozen Elephant Trunk Procedure With Two Configurations of the Jotec E-Vita Hybrid Graft
NCT number | NCT03600077 |
Other study ID # | FETOPT/18/OSR |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | July 19, 2018 |
Est. completion date | April 30, 2022 |
Verified date | November 2022 |
Source | IRCCS San Raffaele |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
To evaluate two different supra-aortic trunks debranching techniques during open repair of aortic arch aneurysms by means of Frozen Elephant Trunk procedure with two configurations of the Jotec E-Vita hybrid graft.
Status | Completed |
Enrollment | 50 |
Est. completion date | April 30, 2022 |
Est. primary completion date | April 30, 2022 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: patient undergoing treatment of extensive proximal aortic pathology at San Raffaele Hospital since December 2009 Exclusion Criteria: extensive proximal aortic pathology treated by techniques other than frozen elephant trunk : total open aortic repair, total endovascular aortic repair, hybrid endovascular aortic repair in zone 0. |
Country | Name | City | State |
---|---|---|---|
Italy | San Raffaele Hospital | Milano |
Lead Sponsor | Collaborator |
---|---|
IRCCS San Raffaele |
Italy,
Di Eusanio M, Borger M, Petridis FD, Leontyev S, Pantaleo A, Moz M, Mohr F, Di Bartolomeo R. Conventional versus frozen elephant trunk surgery for extensive disease of the thoracic aorta. J Cardiovasc Med (Hagerstown). 2014 Nov;15(11):803-9. doi: 10.2459/ — View Citation
Hagl C, Pichlmaier M, Khaladj N. Elephant trunks in aortic surgery: fresh and frozen. J Thorac Cardiovasc Surg. 2013 Mar;145(3 Suppl):S98-102. doi: 10.1016/j.jtcvs.2012.11.065. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Extracorporeal circulation times (minutes) | - Extracorporeal circulation time | Intraoperative | |
Primary | antegrade cerebral perfusion time (minutes) | - antegrade cerebral perfusion time | Intraoperative | |
Primary | Lower limb perfusion time (minutes) | - Lower limb perfusion time | Intraoperative | |
Secondary | Clinical 30-day results (Percent of participants with the clinical outcome) | - Mortality (%) | Perioperative, 30 days | |
Secondary | Clinical 30-day results (Percent of participants with the clinical outcome) | - Stroke (%) | Perioperative, 30 days | |
Secondary | Clinical 30-day results (Percent of participants with the clinical outcome) | - Spinal cord ischemia ( %) | Perioperative, 30 days | |
Secondary | Clinical 30-day results (Percent of participants with the clinical outcome) | - Prolonged mechanical ventilation: >48h ( %) | Perioperative, 30 days | |
Secondary | Clinical 30-day results (Percent of participants with the clinical outcome) | - Renal impairment (%) | Perioperative, 30 days |