"Percutaneous Axillary Access in the Endovascular Treatment of Thoracoabdominal Aortic Pathology" (PAXA) (PAXA)

December 14, 2020 updated by: Bertoglio Luca, IRCCS San Raffaele

"Percutaneous Axillary Access in the Endovascular Treatment of Thoracoabdominal Aortic Pathology"

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

Study Overview

Status

Completed

Detailed Description

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:

  1. patency of both potential upper extremity access vessels (right/left subclavian artery);
  2. diameter of the proximal axillary artery on both sides;
  3. diameter of the distal axillary artery on both sides;
  4. presence of calcifications on the proximal axillary artery on both sides;
  5. presence of calcifications on the distal axillary artery on both sides;
  6. arterial tortuosity index on both sides: measured as the ratio between the axillary artery length measured on curved reconstruction and its length measured on 3D reconstruction.

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.

Study Type

Observational

Enrollment (Actual)

50

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Milano, Italy, 20132
        • San Raffaele Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

patient undergoing total endovascular treatment of thoracoabdominal pathology

Description

Inclusion criteria:

• Patient undergoing total endovascular treatment of thoracoabdominal pathology at San Raffaele Hospital in between October 2013 and December 2020.

Exclusion criteria:

• Incomplete imaging quality not including the arterial segments to be studied (axillary and brachial artery).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Use of upper extremity access in endovascular repair of thoracoabdominal aortic aneurysms
Time Frame: between 2013 and 2020
  • Endovascular graft design : branched / fenestrated
  • Employment of UEA(upper extremity arterial access ) during TAAA endovascular repair: yes / no
  • Side of UEA(upper extremity arterial access ) cannulation (left / right)
  • Site of UEA(upper extremity arterial access ) cannulation:proximal axillary artery / distal axillary artery / upper brachial artery.
  • Size of percutaneuos access sheath employed measured in French - Fr
  • Number of percutaneuos access vessel closure devices employed
  • Access closure specific outcome: primary success / secondary success / failure As reported on patients' charts and operative report
between 2013 and 2020

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Upper extremity access vascular anatomy
Time Frame: between 2013 and 2017.
  • UEA(upper extremity arterial access ) vessel patency: yes / no
  • Diameter of proximal axillary artery measured in Millimeters ( mm)
  • Diameter of distal axillary artery measured in Millimeters (mm)
  • Presence of calcifications at UEA(upper extremity arterial access ): none / < 50% / > 50%.
  • Tortuosity index reported as bare number, defined as the ratio between the axillary artery length measured on curved centerline reconstruction and its length measured on 3D reconstruction.

As measured at preoperative contrast-enhanced CT scan

between 2013 and 2017.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Luca Bertoglio, MD, San Raffaele Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 28, 2017

Primary Completion (Actual)

December 14, 2020

Study Completion (Actual)

December 14, 2020

Study Registration Dates

First Submitted

July 7, 2017

First Submitted That Met QC Criteria

July 17, 2017

First Posted (Actual)

July 21, 2017

Study Record Updates

Last Update Posted (Actual)

December 16, 2020

Last Update Submitted That Met QC Criteria

December 14, 2020

Last Verified

December 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • PAXA/31/OSR

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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