1. Inositol in the MAnaGemENt of abdominal aortic aneurysm (IMAGEN): study protocol for a randomised controlled trial
- Author
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Jenna Pinchbeck, Susan K. Morton, Joseph V. Moxon, Corey S. Moran, T. Christian Gasser, Christopher M. Reid, Lisan Yip, Ramesh Velu, Michael J. Bourke, Jason Jenkins, Georgina Anderson, Bernie Bourke, Rene Jaeggi, Sophie E. Rowbotham, and Jonathan Golledge
- Subjects
medicine.medical_specialty ,Medicine (miscellaneous) ,macromolecular substances ,030204 cardiovascular system & hematology ,Placebo ,Computed tomographic ,law.invention ,Study Protocol ,03 medical and health sciences ,0302 clinical medicine ,Clinical Protocols ,Double-Blind Method ,Randomized controlled trial ,law ,Informed consent ,medicine.artery ,Outcome Assessment, Health Care ,medicine ,Humans ,Pharmacology (medical) ,Prospective Studies ,cardiovascular diseases ,030212 general & internal medicine ,Prospective cohort study ,lcsh:R5-920 ,business.industry ,Abdominal aorta ,medicine.disease ,Abdominal aortic aneurysm ,3. Good health ,Surgery ,Clinical trial ,cardiovascular system ,lcsh:Medicine (General) ,business ,Inositol ,Aortic Aneurysm, Abdominal - Abstract
Background An abdominal aortic aneurysm (AAA) is a focal dilation of the abdominal aorta and is associated with a risk of fatal rupture. Experimental studies suggest that myo-inositol may exert beneficial effects on AAAs through favourable changes to biological pathways implicated in AAA pathology. The aim of the Inositol in the MAnaGemENt of abdominal aortic aneurysm (IMAGEN) trial is to assess if myo-inositol will reduce AAA growth. Methods/design IMAGEN is a multi-centre, prospective, parallel-group, randomised, double-blind, placebo-controlled trial. A total of 164 participants with an AAA measuring ≥ 30 mm will be randomised to either 2 g of myo-inositol or identical placebo twice daily for 12 months. The primary outcome measure will be AAA growth estimated by increase in total infrarenal aortic volume measured on computed tomographic scans. Secondary outcome measures will include AAA diameter assessed by computed tomography and ultrasound, AAA peak wall stress and peak wall rupture index, serum lipids, circulating AAA biomarkers, circulating RNAs and health-related quality of life. All analysis will be based on the intention-to-treat principle at the time of randomisation. All patients who meet the eligibility criteria, provide written informed consent and are enrolled in the study will be included in the primary analysis, regardless of adherence to dietary allocation. Discussion Currently, there is no known medical therapy to limit AAA progression. The IMAGEN trial will be the first randomised trial, to our knowledge, to assess the value of myo-inositol in limiting AAA growth. Trial registration Australian New Zealand Clinical Trials Registry, ACTRN12615001209583. Registered on 6 November 2015. Electronic supplementary material The online version of this article (doi:10.1186/s13063-017-2304-x) contains supplementary material, which is available to authorized users.
- Published
- 2017