RECRUITING

Branched Aortic Arch Study

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a study to assess the safety and effectiveness of endovascular treatment of aortic aneurysms involving the proximal aortic arch. The investigational operation involves placing a stent-graft over the aortic aneurysm.

Official Title

Branched Stent-Graft Repair for Endo Repair of Aneurysms Involving the Proximal Aortic Arch

Quick Facts

Study Start:2006-10
Study Completion:2024-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT00488696

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Aneurysm of the aortic arch larger than 6cm in diameter, or symptomatic aneurysm of the aortic arch, of any diameter, or any arch aneurysm with a 2-year rupture rate estimated to be more than 20%.
  2. * Anticipated mortality rate with open repair estimated to be more than 20%.
  3. * Suitable arterial anatomy for stent-graft
  4. * Life expectancy more than 2 years
  5. * Ability to give informed consent and willingness to comply with follow-up schedule
  1. * Free rupture of the aneurysm
  2. * Pregnancy
  3. * Anaphylactic reaction to contrast material
  4. * Allergy to stainless steel or polyester
  5. * Unwillingness or inability to comply with the follow-up schedule
  6. * Serious systemic or groin infection
  7. * Uncorrectable coagulopathy
  8. * Significant presence of carotid artery atherosclerosis
  9. * Arrhythmia define as 2nd- and 3rd-degree atrioventricular block or sinus node disease, such as sick sinus syndrome and symptomatic bradycardia, unless the patient already has a pacemaker in place and cardiology consultation confirms that it is safe to proceed.

Contacts and Locations

Study Contact

Linda M Reilly, MD
CONTACT
415-353-4366
linda.reilly2@ucsf.edu
Timothy AM Chuter, MD
CONTACT
415-353-4366
timothy.chuter@ucsf.edu

Principal Investigator

Linda M Reilly, MD
PRINCIPAL_INVESTIGATOR
University of California, San Francisco

Study Locations (Sites)

UCSF Division of Vascular and Endovascular Surgery
San Francisco, California, 94143
United States

Collaborators and Investigators

Sponsor: Timothy Chuter, MD

  • Linda M Reilly, MD, PRINCIPAL_INVESTIGATOR, University of California, San Francisco

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 Registration Dates

Study Start Date2006-10
Study Completion Date2024-12

Study Record Updates

Study Start Date2006-10
Study Completion Date2024-12

Terms related to this study

Keywords Provided by Researchers

  • Aneurysm
  • Aortic Arch
  • Endovascular
  • Stent-Graft

Additional Relevant MeSH Terms

  • Aortic Aneurysm of the Proximal Arch