Treatment in Thoracic Aortic Aneurysm: Surgery vs Surveillance
Condition(s) studied
Investigational drug(s) / intervention(s)
Thoracic Aortic Surgery: Thoracic aortic surgery to treat thoracic aortic aneurysm
Study summary
The ascending aorta conducts blood from the heart to the rest of the body. The ascending aorta can become enlarged, and the risk of tearing and rupturing becomes higher with larger aorta. When the ascending aorta tears or ruptures, the risk dying is high even if surgery is done as soon as possible. Traditionally, when the ascending aorta gets above 5.5 cm, surgery is recommended to replace the aorta. However, this threshold is based relatively weak evidence, and sometimes patients with smaller aorta can tear or rupture. On the other hand, surgery carries its own risk as well. Since there are risk of waiting or doing surgery, there is currently no great support for either approach for patients with a smaller aorta. In the TITAN SvS trial, patients with an ascending aorta between 5.0 to 5.5 cm is assigned by chance to the early surgery group, in which they will undergo replacement of aorta, or the surveillance group, in which they will be closely monitored. The chance of dying or suffer tearing or rupture of aorta between the two groups will be compared. The result of the trial will guide future practice for patients with enlarged ascending aorta.
This is a prospective, multi-centre randomized control trial that compares the all-cause mortality, aneurysm-related aortic events, rate of stroke, and quality of life for those patients undergoing early elective ascending aortic surgery to those patients undergoing surveillance. Patients referred for an ascending aortic aneurysm that meets the inclusion criteria will be randomized to the early elective surgery group or the surveillance group. Recruitment will end when the desired sample size is reached, and the patients will be followed for a minimum 2-year period. The primary objective of the trial is to compare the composite outcome of the all-cause mortality and incidence of acute aortic events between surveillance and elective ascending aortic surgery for patients with degenerative or bicuspid valve-related ascending aortic aneurysm after 2 years of follow up. The hypothesis is that the early surgery group will have a significantly lower all-cause mortality and incidence of acute aortic events at 2 years of follow up compare to the surveillance group. The result of this trial will provide evidence based guidance in the appropriate management of ascending aortic aneurysm based on the size criteria, and establish a large database for future investigations.
Eligibility
Primary outcome measure(s)
- All-cause mortality and incidence of acute aortic events in both surveillance and elective ascending aortic surgery groups for patients with degenerative or bicuspid valve-related ascending aortic aneurysm after 2 years of follow up. — 2 years
At 2 years follow up, number of patients in surveillance versus treatment group suffering from mortality or acute aortic dissection
Trial sites (31)
| Facility | City | Region | Status |
|---|---|---|---|
| University of California at San Francisco Medical Center | San Francisco | California | Recruiting |
| University of Iowa | Iowa City | Iowa | Recruiting |
| Massachusetts General Hospital | Boston | Massachusetts | Recruiting |
| Beth Israel Deaconess Medical Center | Boston | Massachusetts | Recruiting |
| University of Michigan | Ann Arbor | Michigan | Recruiting |
| Mayo Clinic | Rochester | Minnesota | Recruiting |
| Washington University School of Medicine | St Louis | Missouri | Recruiting |
| The Valley Hospital, Inc | Ridgewood | New Jersey | Recruiting |
| Icahn School of Medicine at Mount Sinai | New York | New York | Recruiting |
| Duke University | Durham | North Carolina | Recruiting |
| University Hospitals Cleveland | Cleveland | Ohio | Recruiting |
| Ohio State University Medical Center | Columbus | Ohio | Recruiting |
| The Trustees of the University of Pennsylvania | Philadelphia | Pennsylvania | Recruiting |
| MUSC Health University Medical Center | Charleston | South Carolina | Recruiting |
| University of Texas Health Science Centre | Houston | Texas | Recruiting |
| Baylor Scott & White Research Institute | Plano | Texas | Recruiting |
| University of Calgary | Calgary | Alberta | Active Not Recruiting |
| Mazankowski Alberta Heart Institute | Edmonton | Alberta | Recruiting |
| Horizon Health Network | Saint John | New Brunswick | Recruiting |
| Newfoundland Health Services | St. John's | Newfoundland and Labrador | Recruiting |
| Nova Scotia Health Authority | Halifax | Nova Scotia | Recruiting |
| Health Sciences North | Greater Sudbury | Ontario | Recruiting |
| Hamilton General Hospital | Hamilton | Ontario | Active Not Recruiting |
| London Health Sciences Centre | London | Ontario | Recruiting |
| University of Ottawa Heart Institute | Ottawa | Ontario | Recruiting |
| St. Michael's Hospital | Toronto | Ontario | Not Yet Recruiting |
| Toronto General Hospital | Toronto | Ontario | Recruiting |
| Montreal Heart Institute | Montreal | Quebec | Recruiting |
| McGill University Health Centre | Montreal | Quebec | Recruiting |
| Institut universitaire de cardiologie et de pneumologie de Québec | Québec | Quebec | Recruiting |
| Skåne University Hospital | Malmö | Skåne County | Recruiting |
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT03536312 on ClinicalTrials.gov ↗ ← All trials in Sweden