San Raffaele Hospital
Milan, 20132, Italy
NCT Number: NCT03223311
Since the development of custom-made fenestrated and branched endografts a novel therapeutic option for the management of thoracoabdominal and para-renal aortic aneurysms was made accessible. Because of the design of these branched endografts, an arterial vascular access from the upper limb is required to allow selective catheterization of the branch component and the respective target vessel (celiac trunk, superior mesenteric artery, renal artery).2
Looking for future studies?
Notify Me18 year–80 year
All sexes
Observational
Milan, 20132, Italy
Primary end-point is to evaluate the requirement of upper extremity arterial access (UEA) retrospectively in the cohort of patients with thoracoabdominal aortic aneurysms treated by means fenestrated and/or branched endografts in Vascular surgery San Raffaele Hospital between 2013 and 2017, and prospectively in the next 50 patients that will be treated between 2017 and 2020.
Secondary end-point is an anatomical evaluation of the different sites available for UEA(upper extremity arterial access ) based on pre-operative imaging studies.
Materials and methods:
The investigators review a prospectively compiled Microsoft Office Excel database with the procedural details of the 34 patients treated at Vascular surgery of San Raffaele Hospital between October 2013 and March 2017 by means of total endovascular thoracoabdominal aortic aneurysm repair and of those of the next 50 patients who will be treated until December 2020. All patients in which an UAE (upper extremity arterial access ) is employed will be identified together with the side (left/right) and site (proximal/distal axillary artery, brachial artery) of vascular access. Furthermore, the pre-operative contrast-enhanced computed tomography scans (CTA) of all patients, stored in the hospital PACS, will be analyzed on the dedicated workstation with OsiriX software (Pixmeo sarl, Bernex, Switzerland) currently employed at Vascular surgery of San Raffaele Hospital for imaging assessment.
Requirement of an UEA(upper extremity arterial access ) during the procedure is extrapolated from the corresponding field of the available database and reported together with side and site of access and reason for the employment of UEA (upper extremity arterial access ) and for its location.
Multi-planar, curved and 3D reconstructions of each patient CTA will be analyzed and the following measurements recorded:
All the assessed variables will be prospectively recorded in a Microsoft Office Excel database together with patients' weight, height, age and gender.
All patients involved in the retrospective part of the study have already signed informed consent for data collection and analysis at hospital admission.
The 50 patients that will be enrolled until December 2020 will also sign an "ad hoc" consents, specific for this study.
Sensitive patient information will not be available during data analysis. The clinical study will be carried out according to the ethical principles of the Declaration of Helsinki and following the active regulations on observational studies.
Analysis:
Patients characteristics and anatomical data on UEAs(upper extremity arterial access) will be analyzed on Wizard Statistics software to investigate the presence of statistically significant Pearson correlations among the identified variables.
The extracted data and their relevant clinical and procedural implications will be submitted for publication in peer-reviewed scientific journals focused on the field of vascular and endovascular surgery.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: between 2013 and 2020
Time frame: between 2013 and 2017.
As measured at preoperative contrast-enhanced CT scan
IRCCS San Raffaele
Other
"Percutaneous Axillary Access in the Endovascular Treatment of Thoracoabdominal Aortic Pathology"
Acronym: PAXA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04731636
Aneurysm, Aortic Aneurysm
Beijing, Beijing Municipality, China
View Trial DetailsNCT05956873
Aneurysm, Aneurysm, Ruptured
Bologna, Emilia-Romagna, Italy
View Trial DetailsNCT02528500
Aneurysm, Aortic Aneurysm
Rochester, Minnesota, United States
View Trial DetailsNCT01756911
Aneurysm, Aortic Aneurysm
Besançon, France
View Trial Details