Patients With an Abdominal Aortic Aneurysm of 39-49 mm in Diameter Clinical Trial
Official title:
The Intervention Effect Of Alpha-Ketoglutarate On Abdominal Aortic Aneurysm Progression and Rupture: A Prospective, Randomized Parallel Controlled Study Based On Large Cohorts
Verified date | February 2021 |
Source | RenJi Hospital |
Contact | Jun Pu |
Phone | 86-21-68383477 |
pujun310[@]hotmail.com | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this project is to define whether nutritional supplement (oral administration with alpha-ketoglutarate) capable of filling-up the citric acid cycle (anaplerotic therapy) can improve outcomes in patients with an abdominal aortic aneurysm of 39-49 mm in diameter on ultrasound imaging. Alpha-ketoglutarate is commonly used as a nutritional supplement specially by athletes to increase muscle strength. They can be mixed with formula or other foods. Subjects will be followed for up to 5 years.
Status | Recruiting |
Enrollment | 300 |
Est. completion date | December 31, 2026 |
Est. primary completion date | February 1, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 50 Years and older |
Eligibility | Inclusion Criteria: 1. Presence of an infrarenal AAA with a maximum diameter of 39-49 mm; 2. Han nationality; 3. Between 50 years or more, no gender limit; 4. No mental illness; 5. No history of supplement allergy or supplement allergy; 6. Subjects voluntarily participate in this study, sign an informed consent form, have good compliance, and cooperate with follow-up. Exclusion Criteria: 1. Previous infrarenal aortic surgery; 2. Planned major surgery; 3. Known aortic dissection; 4. Have received any other clinical trial treatment within 1 year; 5. Systemic treatment with corticosteroids or other systemic immunomodulatory therapy; 6. Severe infections, including but not limited to infections requiring hospitalization, bacteremia, severe pneumonia, etc.; 7. Known or suspected inherited connective tissue disorder; 8. Calculated creatinine clearance of less than 30 ml/min; 9. Known significant liver disease; 10. Known human immunodeficiency virus infection at the time of screening; 11. Serious concomitant illness associated with life expectancy of less than 2 years; 12. Any other significant and unstable condition that could limit compliance with the trial protocol. |
Country | Name | City | State |
---|---|---|---|
China | Cardiology, Ren Ji Hospital | Shanghai |
Lead Sponsor | Collaborator |
---|---|
RenJi Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in aortic diameter | Measure the aortic diameter by ultrasound imaging from leading edge adventitia at the anterior wall to leading edge adventitia at the posterior wall. | 1 year | |
Secondary | Rates of AAA repair/rupture | Calculate the incidence of AAA repair/rupture | 1 year | |
Secondary | Rates of mortality | Calculate the mortality due to AAA rupture | 1 year | |
Secondary | Changes level of plasma biomarker | Measure plasma levels of tryptase | 1 year |