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Incidence of Major Complication in Case of Thoracic Aortic Aneurysm (MOTAAR)

U

University Hospital, Lille

Status

Enrolling

Conditions

Thoracic Aortic Aneurysm

Study type

Observational

Funder types

Other

Identifiers

NCT05395598
2021_0151
2022-A00439-34 (Other Identifier)

Details and patient eligibility

About

Thoracic aneurysm is a silent disease with a potential mid-term high risk of death or major complications. Few data are available on the real incidence of major complications in case of small and moderate thoracic aneurysm. Different factors are supposed to increase the risk of aortic enlargement as high blood pressure and sleep disorder breathing. The modality of imaging and clinical follow-up are well defined. In this prospective observational study, the aim to assess the incidence of of major complications during follow-up in a population of patients with a small or moderate thoracic aneurysm. The study will also try to identify systemic factors influencing aneurysm evolution.

Enrollment

320 estimated patients

Sex

All

Ages

45 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Documentation of an aortic root aneurysm > 40 mm
  • Agreement to participate to a longitudinal study and available for a 5 years follow-up

Exclusion criteria

  • Presence of comorbidities or pathology with a prognosis of less than 1 year
  • Personal or family history of genetically documented elastic tissue disease or patient meeting the GAND clinical criteria suggestive of Marfan disease
  • High-grade mitra-aortic valve disease, even if asymptomatic
  • Unbalanced hypertension ≥ 180/110 mmHg
  • Aneurysm (regardless of thoracic or abdominal location) ≥ 50 mm
  • Aneurysm (regardless of thoracic or abdominal location) with documented progression of more than 5 mm over one year
  • History of aortic surgery or endovascular intervention and history of type B aortic dissection of medical treatment
  • Renal insufficiency on dialysis, or GFR< 30 ml/mn (CKD-EPI)

Trial contacts and locations

1

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Central trial contact

Pascal DELSART, MD

Data sourced from clinicaltrials.gov

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