Actively Recruiting
Treatment in Thoracic Aortic Aneurysm: Surgery vs Surveillance
Led by Ottawa Heart Institute Research Corporation · Updated on 2025-09-22
610
Participants Needed
28
Research Sites
873 weeks
Total Duration
On this page
Sponsors
O
Ottawa Heart Institute Research Corporation
Lead Sponsor
U
University of Calgary
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Treatment in Thoracic Aortic Aneurysm: Surgery vs Surveillance
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients between the age of 18 and 79 inclusive
- Ascending aortic aneurysm between 5.0 cm and 5.4 cm in maximal diameter as measured by CT with contrast
- Patients with ascending aortic aneurysm with a diameter of 4.5 cm to 4.9 cm will be observed with serial CT and considered for enrollment once the aneurysm reaches 5.0 cm
You will not qualify if you...
- Patients who refused to be randomized
- Patients with symptoms attributable to ascending aortic aneurysms
- Patients unable to provide informed consent
- Patients unable to attend regular follow-up or comply with the protocol
- Previous cardiac surgery
- Patients whose primary indication for cardiac surgery is not related to ascending aortic aneurysm
- Known aneurysm expansion rate exceeding 0.5 cm per year during the past 5 years
- Arch aneurysms without ascending aorta involvement
- Ascending aortic and arch aneurysm with descending thoracic aorta involvement
- Known connective tissue diseases (e.g., Marfan syndrome, Loey-Dietz syndrome, Turner syndrome)
- Possible genetic aortopathies such as family history of aortic aneurysms or premature aortic dissections/ruptures
- Inflammatory arteritis (e.g., Takayasu's arteritis, syphilitic arteritis)
- Female patients who are pregnant or planning to become pregnant
- History or presence of medical, psychiatric, or other conditions that would make the patient ineligible
- Patients deemed unfit for surgery due to severe pulmonary disease, creatinine ≥ 250 µmol/L, Child Pugh Class B or C, NYHA class III or IV, recent myocardial infarction within 6 months, major surgery or angioplasty within 3 months, or expected survival less than 5 years due to other diseases
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 28 locations
1
University of California at San Francisco Medical Center
San Francisco, California, United States, 94121
Actively Recruiting
2
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114
Actively Recruiting
3
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States, 02215
Actively Recruiting
4
University of Michigan
Ann Arbor, Michigan, United States, 48109
Actively Recruiting
5
Mayo Clinic
Rochester, Minnesota, United States, 55905
Actively Recruiting
6
Washington University School of Medicine
St Louis, Missouri, United States, 63110
Actively Recruiting
7
The Valley Hospital, Inc
Ridgewood, New Jersey, United States, 07652
Actively Recruiting
8
Icahn School of Medicine at Mount Sinai
New York, New York, United States, 10029
Actively Recruiting
9
Duke University
Durham, North Carolina, United States, 27705
Actively Recruiting
10
University Hospitals Cleveland
Cleveland, Ohio, United States, 44106
Actively Recruiting
11
Ohio State University Medical Center
Columbus, Ohio, United States, 43210
Actively Recruiting
12
The Trustees of the University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
13
MUSC Health University Medical Center
Charleston, South Carolina, United States, 29425
Actively Recruiting
14
University of Texas Health Science Centre
Houston, Texas, United States, 77030
Actively Recruiting
15
Baylor Scott & White Research Institute
Plano, Texas, United States, 75093
Actively Recruiting
16
University of Calgary
Calgary, Alberta, Canada, T2N 2T9
Actively Recruiting
17
Mazankowski Alberta Heart Institute
Edmonton, Alberta, Canada, T6G 0M9
Actively Recruiting
18
Horizon Health Network
Saint John, New Brunswick, Canada, E2L 4L2
Actively Recruiting
19
Nova Scotia Health Authority
Halifax, Nova Scotia, Canada, B3S 0H6
Actively Recruiting
20
Health Sciences North
Greater Sudbury, Ontario, Canada
Actively Recruiting
21
Hamilton General Hospital
Hamilton, Ontario, Canada
Actively Recruiting
22
London Health Sciences Centre
London, Ontario, Canada, N6A 5A5
Actively Recruiting
23
University of Ottawa Heart Institute
Ottawa, Ontario, Canada, K1Y 4W7
Actively Recruiting
24
St. Michael's Hospital
Toronto, Ontario, Canada, M5B 1W8
Not Yet Recruiting
25
Toronto General Hospital
Toronto, Ontario, Canada
Actively Recruiting
26
Montreal Heart Institute
Montreal, Quebec, Canada, H1T 1C8
Actively Recruiting
27
McGill University Health Centre
Montreal, Quebec, Canada, H3H2R9
Actively Recruiting
28
Institut universitaire de cardiologie et de pneumologie de Québec
Québec, Quebec, Canada, G1V 4G5
Actively Recruiting
Research Team
K
Khatira Mehdiyeva
CONTACT
A
Alice Black
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here