Endovascular Exclusion of Thoracoabdominal and/or Paravisceral Abdominal Aortic Aneurysm
Primary Purpose
Thoracoabdominal Aortic Aneurysm, Paravisceral Abdominal Aortic Aneurysm
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Endovascular Branched Stent-Graft
Sponsored by
About this trial
This is an interventional treatment trial for Thoracoabdominal Aortic Aneurysm focused on measuring Thoracoabdominal, Paravisceral, Aneurysm, Endovascular, Stent-Graft, Aorta
Eligibility Criteria
Inclusion Criteria
Aortic aneurysms:
- greater than or equal to 6 cm in diameter in men,
- greater than or equal to 5.5 cm in diameter in women,
- and/or larger than 5 cm in diameter and enlarging at a rate of more than 5 mm/year,
- and/or iliac aneurysms larger than 4 cm in diameter.
- Anticipated mortality comparable to published rates with conventional surgical treatment.
- Life expectancy more than 2 years.
- Ability to give informed consent.
- Willingness to comply with follow-up schedule.
- Suitable arterial anatomy for endovascular repair.
Exclusion Criteria
- Free rupture of the aneurysm.
- Pregnancy.
- Known allergy to Nitinol, stainless steel, or polyester.
- Unwillingness or inability to comply with the follow up schedule.
- Serious systemic or groin infection.
- Uncorrectable coagulopathy.
Sites / Locations
- Division of Vascular Surgery, SFVAMCRecruiting
- Division of Vascular Surgery, UCSFRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Interventional
Arm Description
Endovascular Branched Stent-Graft: The investigational operation is done making small incisions in both groins and the right arm and placing a graft in the aorta through tubes that are inserted through the femoral and brachial arteries, than fastening it in position with metal springs(stents).
Outcomes
Primary Outcome Measures
Successful implantation of TAAA branched stent-graft.
Secondary Outcome Measures
Long term success of TAAA branched stent-graft treatment.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00483249
Brief Title
Endovascular Exclusion of Thoracoabdominal and/or Paravisceral Abdominal Aortic Aneurysm
Official Title
Endovascular Exclusion of Thoracoabdominal and/or Paravisceral Abdominal Aortic Aneurysm
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 2005 (undefined)
Primary Completion Date
December 2026 (Anticipated)
Study Completion Date
December 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Timothy Chuter, MD
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is a study to assess the safety and effectiveness of endovascular treatment of thoracoabdominal (TAAA) and paravisceral abdominal (PVAAA) aortic aneurysms. The investigational operation involves placing a stent-graft over the aortic aneurysm.
Detailed Description
A TAAA or PVAAA is an abnormal enlargement of the aorta, the main artery in the chest and abdomen. The standard operation for TAAA of PVAAA is performed through a long incision extending down the side of the chest and the front of the abdomen. In the standard operation, the weak area of the aorta is replaced with a fabric sleeve (graft). The investigational operation is done making small incisions in both groins and the right arm and placing a graft in the aorta through tubes that are inserted through the femoral and brachial arteries, than fastening it in position with metal springs(stents). The combination of a stent and a graft is known as a stent-graft. Compared with standard operation, the potential advantages of endovascular TAAA/PVAAA repair include less pain, less disturbance of intestinal function, a lower risk of pulmonary or cardiac complications and shorter hospital stay. The main disadvantage of endovascular TAAA/PVAAA is an unknown success rate.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thoracoabdominal Aortic Aneurysm, Paravisceral Abdominal Aortic Aneurysm
Keywords
Thoracoabdominal, Paravisceral, Aneurysm, Endovascular, Stent-Graft, Aorta
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
250 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Interventional
Arm Type
Experimental
Arm Description
Endovascular Branched Stent-Graft: The investigational operation is done making small incisions in both groins and the right arm and placing a graft in the aorta through tubes that are inserted through the femoral and brachial arteries, than fastening it in position with metal springs(stents).
Intervention Type
Device
Intervention Name(s)
Endovascular Branched Stent-Graft
Intervention Description
Industry manufactured branched stent-graft for treatment of TAAA/PVAAA.
Primary Outcome Measure Information:
Title
Successful implantation of TAAA branched stent-graft.
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Long term success of TAAA branched stent-graft treatment.
Time Frame
5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria
Aortic aneurysms:
greater than or equal to 6 cm in diameter in men,
greater than or equal to 5.5 cm in diameter in women,
and/or larger than 5 cm in diameter and enlarging at a rate of more than 5 mm/year,
and/or iliac aneurysms larger than 4 cm in diameter.
Anticipated mortality comparable to published rates with conventional surgical treatment.
Life expectancy more than 2 years.
Ability to give informed consent.
Willingness to comply with follow-up schedule.
Suitable arterial anatomy for endovascular repair.
Exclusion Criteria
Free rupture of the aneurysm.
Pregnancy.
Known allergy to Nitinol, stainless steel, or polyester.
Unwillingness or inability to comply with the follow up schedule.
Serious systemic or groin infection.
Uncorrectable coagulopathy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Warren J Gasper, MD
Phone
415 750 2115
Email
warren.gasper@ucsf.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Linda M Reilly, MD
Phone
415 353 4366
Email
linda.reilly2@ucsf.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Warren J Gasper, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
Division of Vascular Surgery, SFVAMC
City
San Francisco
State/Province
California
ZIP/Postal Code
94121
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Warren J Gasper, MD
First Name & Middle Initial & Last Name & Degree
Linda M Reilly, MD
Facility Name
Division of Vascular Surgery, UCSF
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Linda M Reilly, MD
First Name & Middle Initial & Last Name & Degree
Warren J Gasper, MD
First Name & Middle Initial & Last Name & Degree
Timothy AM Chuter, MD
First Name & Middle Initial & Last Name & Degree
Jade S Hiramoto, MD
First Name & Middle Initial & Last Name & Degree
Shant M Vartanian, MD
12. IPD Sharing Statement
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Learn more about this trial
Endovascular Exclusion of Thoracoabdominal and/or Paravisceral Abdominal Aortic Aneurysm
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