Inclusion criteria |
• Ability to provide written informed consent |
• Diagnosis with an infrarenal AAA measuring a maximum diameter ≥ 30 mm based on CT or ultrasound |
• No current indication for AAA repair according to the treating physician or expectation that this will be revised over 12 months |
• High likelihood of treatment compliance over 12 months according to the treating physician and local study coordinator |
• Aged ≥ 50 years |
Exclusion criteria |
• Symptomatic, ruptured or mycotic AAA |
• Contraindication to the study protocol: |
â—‹ Previous reaction to myo-inositol supplementation |
â—‹ Inability to tolerate abdominal imaging |
â—‹ Inability to provide blood samples for safety and outcome analysis |
• Previous abdominal aortic surgery |
• Current or planned participation in another randomised trial |
• Treating physician feels the patient is not suitable for trial entry |