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IMAGEN: Effect of a dietary supplement on abdominal aortic aneurysm (AAA) growth

Effect of a dietary supplement on abdominal aortic aneurysm (AAA) growth assessed by determining changes in AAA volume by CT imaging.

Status
Suspended
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615001209583
Acronym
IMAGEN
Enrollment
75
Registered
2015-11-06
Start date
2016-01-13
Completion date
2017-02-24
Last updated
2026-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

IMAGEN is a multicentre, prospective, parallel group, randomised, double-blinded placebo-controlled trial to assess if 4g of a dietary supplement daily over 12 months will reduce AAA growth. Participants who consent will undergo a thorough screening assessment for safety and suitability. Assessments include; physical and clinical examination, blood test, CT and Ultrasound of the abdomen, quality of life questionnaire and diet assessment. If the participants meet all inclusion criteria and no exclusion criteria they will be randomised (randomly allocated) to either the dietary supplement or placebo group. The participant will be blinded to the supplement name and it will be referred to as "the supplement" from the moment of initial contact. The dietary supplement and a placebo equivalent powder will be separately packaged in 500mg dose capsules. The capsules will be dispensed by an independent and unblinded pharmacist. Participants will be instructed to have four 500mg capsules twice per day at 8am and 8pm. Participants will revisit the site centre at 6 and 12 months after starting the trial to monitor adverse events, compliance and perform assessments. Participants will be contacted by telephone at 1, 3 and 9 months to monitor compliance and adverse events. The team will consist of experienced investigators, vascular surgeons, coordinators and researchers at each site. A steering committee, data and safety committee and publications committee will be established to oversee various aspects of the study to ensure the aims of the study are met while upholding the protocol

Interventions

Oral administration of 2g of a dietary supplement twice daily for 12 months. Drug capsule return and control diary will monitor adherence.

Sponsors

James Cook University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

The study will include patients who provide written informed consent and have the following eligibility criteria: - An infrarenal AAA measuring a minimal diameter of 30 mm on ultrasound or CT - No current indication for AAA repair according to the treating physician - High likelihood of compliance with treatment over 12 months according to the treating physician and local study coordinator

Exclusion criteria

The following exclusion criteria will be used: - Symptomatic, ruptured or infected AAAs - Previous abdominal aortic surgery - Current participation in another randomised trial - The treating physician feels the patient is not suitable for trial entry

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 14, 2026