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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04224051
Other study ID # MAAAGI
Secondary ID
Status Enrolling by invitation
Phase Phase 2
First received
Last updated
Start date February 12, 2020
Est. completion date January 2026

Study information

Verified date September 2023
Source Uppsala University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 500
Est. completion date January 2026
Est. primary completion date January 2026
Accepts healthy volunteers No
Gender All
Age group 50 Years to 80 Years
Eligibility 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.

Study Design


Intervention

Drug:
Metformin
Metformin target dose 2 g daily
Other:
Standard care
Abdominal aortic aneurysm surveillance

Locations

Country Name City State
Sweden Uppsala University Hospital Uppsala Sverige

Sponsors (1)

Lead Sponsor Collaborator
Uppsala University Hospital

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Abdominal aortic aneurysm (AAA) diameter growth rate 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. 5 years
Secondary Abdominal aortic aneurysm (AAA) volume growth rate 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. 5 years
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