MAAAGI: Metformin for Abdominal Aortic Aneurysm Growth Inhibition

Sponsor
Uppsala University Hospital (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT04224051
Collaborator
(none)
500
1
2
70.6
7.1

Study Details

Study Description

Brief Summary

A multi-centre population-based open-label randomized controlled trial with allocation concealment and blinded outcome assessment will examine if up to 2g metformin daily slows AAA growth in patients with small AAAs who do not have diabetes.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Subjects with no history of diabetes will be recruited from a cohort of patients with diagnosed AAA and a maximum aortic diameter of 30-49mm for men and 30-44mm for women.

A total of 500 subjects with AAA will be included in the study, 250 in each study arm. Patients will be randomised to metformin or standard care in a 1:1 ratio.

CT imaging and AAA US will be performed at baseline, 24 months and end of study, as well as if necessary according to clinical routine. Study drug will start at baseline and continue through completion.

When all enrolled subjects have completed the 24-month follow-up (including imaging) an interim analysis will be performed to assess for efficacy and safety; if there is no trend towards a positive effect or signs of a harmful effect of metformin, the study will be stopped at this phase.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Metformin for AAA Growth Inhibition, a Randomized Controlled Trial
Actual Study Start Date :
Feb 12, 2020
Anticipated Primary Completion Date :
Jan 1, 2026
Anticipated Study Completion Date :
Jan 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Metformin target dose of 2g daily

Metformin tablets taken orally with target dose of 2g daily plus standard care

Drug: Metformin
Metformin target dose 2 g daily

Active Comparator: Standard care

Standard care includes help with smoking cessation if applicable; encouragement of physical activity and a healthy diet; blood pressure control; statin and anti-platelet therapy treatment if the patient have clinical manifestations of atherosclerotic disease.

Other: Standard care
Abdominal aortic aneurysm surveillance

Outcome Measures

Primary Outcome Measures

  1. Abdominal aortic aneurysm (AAA) diameter growth rate [5 years]

    To examine if up to 2g metformin administered daily over a five-year period slows AAA growth measured as computed tomography (CT) imaging assessed AAA diameter (mm) in patients with small AAAs who do not have diabetes.

Secondary Outcome Measures

  1. Abdominal aortic aneurysm (AAA) volume growth rate [5 years]

    To examine if up to 2g metformin administered daily over a five-year period slows AAA growth measured as computed tomography (CT) imaging assessed AAA volume (ml) in patients with small AAAs who do not have diabetes.

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Provision of written informed consent.

  2. Male and female patients.

  3. Age 50-80 years.

  4. Documented AAA Ø 30-49 mm for men and 30-44 mm for women.

  5. Fasting p-glucose <7.0 mmol/L. Fasting is defined as no caloric intake for ≥8 h.

Exclusion Criteria:
  1. Short expected survival.

  2. History of current or previous diabetes mellitus.

  3. Current or previous use of metformin.

  4. Not expected to tolerate metformin.

  5. Contraindications to metformin treatment according to SmPC

  6. Known or suspected connective tissue disorder (Marfans syndrome, etc), infected or inflammatory aneurysm, aneurysm development after aortic dissection or previous surgery of the infrarenal aorta.

  7. Enrollment in either another investigational drug or medical device study or another investigational study of an approved drug or medical device within 30 days prior to enrollment of the current study.

  8. If, in the opinion of the investigator, it is not in the patient's medical interest to participate in the study or the patient is unlikely to be able to comply with the study protocol.

  9. Pregnancy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Uppsala University Hospital Uppsala Sverige Sweden

Sponsors and Collaborators

  • Uppsala University Hospital

Investigators

  • Principal Investigator: Jon Unosson, PhD, Uppsala University Hospital

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Jon Unosson, MD PhD, Uppsala University Hospital
ClinicalTrials.gov Identifier:
NCT04224051
Other Study ID Numbers:
  • MAAAGI
First Posted:
Jan 13, 2020
Last Update Posted:
Sep 30, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 30, 2021