Endovascular Exclusion of Thoracoabdominal and/or Paravisceral Abdominal Aortic Aneurysm
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Thoracoabdominal Aortic Aneurysm Paravisceral Abdominal Aortic Aneurysm |
Device: Endovascular Branched Stent-Graft |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Endovascular Exclusion of Thoracoabdominal and/or Paravisceral Abdominal Aortic Aneurysm |
- Successful implantation of TAAA branched stent-graft. [ Time Frame: 1 month ] [ Designated as safety issue: Yes ]
- Long term success of TAAA branched stent-graft treatment. [ Time Frame: 5 years ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 120 |
| Study Start Date: | May 2005 |
| Estimated Primary Completion Date: | December 2014 (Final data collection date for primary outcome measure) |
-
Device: Endovascular Branched Stent-Graft
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.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Aneurysm >6cm in diameter or >5cm in diameter which is enlarging at a rate of >10mm/year
- Anticipated mortality > 20% with conventional surgical treatment
- Life expectancy > 2 years
- Absence of a dominant artery to the spinal cord arising from the are of stent-graft implantation
- Ability to give informed consent and willingness to comply with follow-up schedule
- Suitable arterial anatomy for endovascular repair
Exclusion Criteria:
- Free rupture of the aneurysm
- Pregnancy
- Anaphylactic reaction to contrast material
- Allergy to stainless steel or polyester
- Unwillingness or inability to comply with the follow up schedule
- Serious systemic or groin infection
- Uncorrectable coagulopathy
- Inability to give informed consent in English
Contacts and Locations| Contact: Linda M Reilly, MD | 415 353 4366 | linda.reilly@ucsfmedctr.org |
| Contact: Timothy AM Chuter, MD | 415 353 4366 | timothy.chuter@ucsfmedctr.org |
| United States, California | |
| Division of Vascular Surgery, UCSF | Recruiting |
| San Francisco, California, United States, 94143 | |
| Principal Investigator: Timothy AM Chuter, MD | |
| Principal Investigator: Linda M Reilly, MD | |
| Sub-Investigator: Jade S Hiramoto, MD | |
| Division of Vascular Surgery, SFVAMC | Recruiting |
| San Francisco, California, United States, 94121 | |
| Principal Investigator: Joseph H Rapp, MD | |
| Principal Investigator: Timothy AM Chuter, MD | |
| Principal Investigator: Linda M Reilly, MD | |
| Sub-Investigator: Marlene Grenon, MD | |
More Information
Publications:
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | University of California, San Francisco |
| ClinicalTrials.gov Identifier: | NCT00483249 History of Changes |
| Other Study ID Numbers: | H5357-26067 |
| Study First Received: | June 5, 2007 |
| Last Updated: | June 28, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by University of California, San Francisco:
|
Thoracoabdominal Paravisceral Aneurysm Endovascular Stent-Graft |
Additional relevant MeSH terms:
|
Aneurysm Aortic Aneurysm Aortic Aneurysm, Abdominal Aortic Aneurysm, Thoracic |
Vascular Diseases Cardiovascular Diseases Aortic Diseases |
ClinicalTrials.gov processed this record on May 16, 2013