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MuLtibranchEd Graft for OPen RepAir of ThoRacoabdominal Aneurysms

Primary Purpose

Aneurysm Abdominal, Aneurysm Thoracic

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
branched prosthesis for surgical treatment of thoraco-abdominal aortic aneurysms
Sponsored by
IRCCS San Raffaele
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Aneurysm Abdominal

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients aged ≥ 18 years;
  • patients candidates for surgical treatment of thoraco-abdominal aorta of the II and III type sec. Crawford using "TAAA spinal loop graft" "custom made CE equivalent" prosthesis

Exclusion Criteria:

• patients aged ≤ 18 years

Sites / Locations

  • San Raffaele Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

TAAA spinal loop graft

Arm Description

Outcomes

Primary Outcome Measures

number of participants who obtain technical success
number of surviving participants
incidence of thrombosis of the prosthetic branches, visceral arteries and replanted intercostal arteries
freedom from thrombosis of the prosthetic branches,visceral arteries and replanted intercostal arteries
incidence of aneurysmal dilatation of visceral and replanted intercostal arteries
freedom from surgical / endovascular reoperation for aneurysmal dilatation of visceral and replanted intercostal arteries

Secondary Outcome Measures

Full Information

First Posted
June 9, 2020
Last Updated
November 10, 2022
Sponsor
IRCCS San Raffaele
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1. Study Identification

Unique Protocol Identification Number
NCT04430114
Brief Title
MuLtibranchEd Graft for OPen RepAir of ThoRacoabdominal Aneurysms
Official Title
DediCated MuLtibranchEd DacrOn Graft for OPen RepAir of ThoRacoabdominal Aneurysms - CLEOPATRA Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
June 5, 2020 (Actual)
Primary Completion Date
March 1, 2022 (Actual)
Study Completion Date
March 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IRCCS San Raffaele

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of the study is the evaluation of the technical success and clinical outcomes of the surgical treatment of thoraco-abdominal aortic aneurysms treated by Jotec "TAAA spinal loop graft" "custom made "CE equivalent" branched prosthesis, compared with the patient cohort already treated with standard and / or bench-top prostheses Gelweave ™ Coselli Thoracoabdominal Grafts.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aneurysm Abdominal, Aneurysm Thoracic

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TAAA spinal loop graft
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
branched prosthesis for surgical treatment of thoraco-abdominal aortic aneurysms
Intervention Description
Jotec "TAAA spinal loop graft" "custom made CE equivalent" branched prosthesis, compared with the cohort of patients already treated with standard prostheses and / or Gelweave ™ Coselli Thoracoabdominal Grafts.
Primary Outcome Measure Information:
Title
number of participants who obtain technical success
Description
number of surviving participants
Time Frame
12 month
Title
incidence of thrombosis of the prosthetic branches, visceral arteries and replanted intercostal arteries
Description
freedom from thrombosis of the prosthetic branches,visceral arteries and replanted intercostal arteries
Time Frame
12 month
Title
incidence of aneurysmal dilatation of visceral and replanted intercostal arteries
Description
freedom from surgical / endovascular reoperation for aneurysmal dilatation of visceral and replanted intercostal arteries
Time Frame
12 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients aged ≥ 18 years; patients candidates for surgical treatment of thoraco-abdominal aorta of the II and III type sec. Crawford using "TAAA spinal loop graft" "custom made CE equivalent" prosthesis Exclusion Criteria: • patients aged ≤ 18 years
Facility Information:
Facility Name
San Raffaele Hospital
City
Milano
ZIP/Postal Code
20132
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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MuLtibranchEd Graft for OPen RepAir of ThoRacoabdominal Aneurysms

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