Actively Recruiting

Phase Not Applicable
Age: 18Years - 79Years
All Genders
NCT03536312

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

Age: 18Years - 79Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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

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