No support was supplied by pharmaceutical or medical-device companies. Full authorization of the trial was granted by the United Kingdom’s North West Multicentre Research Ethics Committee. The trial was conducted at 33 hospitals that met the criteria for participation in the trial . Trained local coordinators were responsible for recruitment of individuals, data collection, and follow-up. Trial Procedures Patients of both sexes who were at least 60 years of age with an stomach aortic aneurysm measuring at least 5.5 cm in diameter on computed tomography were evaluated for trial participation.

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