Alpha-Ketoglutarate and Abdominal Aortic Aneurysm Progression and Rupture
Primary Purpose
Patients With an Abdominal Aortic Aneurysm of 39-49 mm in Diameter
Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
alpha-ketoglutarate
Sponsored by
About this trial
This is an interventional treatment trial for Patients With an Abdominal Aortic Aneurysm of 39-49 mm in Diameter focused on measuring cohort study
Eligibility Criteria
Inclusion Criteria:
- Presence of an infrarenal AAA with a maximum diameter of 39-49 mm;
- Han nationality;
- Between 50 years or more, no gender limit;
- No mental illness;
- No history of supplement allergy or supplement allergy;
- Subjects voluntarily participate in this study, sign an informed consent form, have good compliance, and cooperate with follow-up.
Exclusion Criteria:
- Previous infrarenal aortic surgery;
- Planned major surgery;
- Known aortic dissection;
- Have received any other clinical trial treatment within 1 year;
- Systemic treatment with corticosteroids or other systemic immunomodulatory therapy;
- Severe infections, including but not limited to infections requiring hospitalization, bacteremia, severe pneumonia, etc.;
- Known or suspected inherited connective tissue disorder;
- Calculated creatinine clearance of less than 30 ml/min;
- Known significant liver disease;
- Known human immunodeficiency virus infection at the time of screening;
- Serious concomitant illness associated with life expectancy of less than 2 years;
- Any other significant and unstable condition that could limit compliance with the trial protocol.
Sites / Locations
- Cardiology, Ren Ji HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
alpha-ketoglutarate Group
Normal Control Group
Arm Description
Take alpha-ketoglutarate supplements, alpha-ketoglutarate 300mg/d mixed with food or drink, for 1 years
Don't take alpha-ketoglutarate supplements
Outcomes
Primary Outcome Measures
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.
Secondary Outcome Measures
Rates of AAA repair/rupture
Calculate the incidence of AAA repair/rupture
Rates of mortality
Calculate the mortality due to AAA rupture
Changes level of plasma biomarker
Measure plasma levels of tryptase
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04723888
Brief Title
Alpha-Ketoglutarate and Abdominal Aortic Aneurysm Progression and Rupture
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
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2021 (Actual)
Primary Completion Date
February 1, 2026 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
RenJi Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
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.
Detailed Description
Abdominal aortic aneurysm (AAA) is an age-related disease that characterized by permanent regional dilation of the abdominal aortae, which results in catastrophic event of rupture and sudden death. Currently, no effective drug to limit the progression or reduce the risk of rupture has been developed.
Metabolic pathways, including glucose metabolism, lipid metabolism, and amino acid metabolism, have indispensable roles in normal and dysfunctional vasculature. The Krebs cycle is responsible for obtaining energy from food in the form of ATP, and ATP is essential for muscle contraction and correct functioning of all organs. Besides, tight control of mitochondrial functions is critical for maintaining metabolism balance.
As an important metabolite in Krebs cycle, alpha-ketoglutarate not only improved energy metabolism, but also extended lifespan and reduced morbidity in aging mice. It is widely used in the market as a nutritional supplement specially by athletes to increase muscle strength. Until now, no obvious toxic and side effects to the body was observed. Given the high bioavailability, we propose that dietary supplementation with alpha-ketoglutarate can improve the outcome in patients with an abdominal aortic aneurysm of 39-49 mm in diameter.
Therefore, the project team intends to establish the abdominal aortic aneurysm rupture risk prediction model in the elderly cohort in the early stage, and randomize groups in patients with an abdominal aortic aneurysm of 39-49 mm in diameter based on whether or not to supplement alpha-ketoglutarate. There are two cohorts: the alpha-ketoglutarate intervention cohort and the parallel control cohort. By observing the efficacy in terms of change in aortic diameter and abdominal aortic aneurysm rupture incidence in the two groups during the follow-up period, it provides evidence-based medical evidence for the future clinical application of alpha-ketoglutarate.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Patients With an Abdominal Aortic Aneurysm of 39-49 mm in Diameter
Keywords
cohort study
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
alpha-ketoglutarate Group
Arm Type
Experimental
Arm Description
Take alpha-ketoglutarate supplements, alpha-ketoglutarate 300mg/d mixed with food or drink, for 1 years
Arm Title
Normal Control Group
Arm Type
No Intervention
Arm Description
Don't take alpha-ketoglutarate supplements
Intervention Type
Dietary Supplement
Intervention Name(s)
alpha-ketoglutarate
Intervention Description
alpha-ketoglutarate supplements
Primary Outcome Measure Information:
Title
Changes in aortic diameter
Description
Measure the aortic diameter by ultrasound imaging from leading edge adventitia at the anterior wall to leading edge adventitia at the posterior wall.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Rates of AAA repair/rupture
Description
Calculate the incidence of AAA repair/rupture
Time Frame
1 year
Title
Rates of mortality
Description
Calculate the mortality due to AAA rupture
Time Frame
1 year
Title
Changes level of plasma biomarker
Description
Measure plasma levels of tryptase
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Presence of an infrarenal AAA with a maximum diameter of 39-49 mm;
Han nationality;
Between 50 years or more, no gender limit;
No mental illness;
No history of supplement allergy or supplement allergy;
Subjects voluntarily participate in this study, sign an informed consent form, have good compliance, and cooperate with follow-up.
Exclusion Criteria:
Previous infrarenal aortic surgery;
Planned major surgery;
Known aortic dissection;
Have received any other clinical trial treatment within 1 year;
Systemic treatment with corticosteroids or other systemic immunomodulatory therapy;
Severe infections, including but not limited to infections requiring hospitalization, bacteremia, severe pneumonia, etc.;
Known or suspected inherited connective tissue disorder;
Calculated creatinine clearance of less than 30 ml/min;
Known significant liver disease;
Known human immunodeficiency virus infection at the time of screening;
Serious concomitant illness associated with life expectancy of less than 2 years;
Any other significant and unstable condition that could limit compliance with the trial protocol.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jun Pu
Phone
86-21-68383477
Email
pujun310@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jun Pu
Organizational Affiliation
RenJi Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cardiology, Ren Ji Hospital
City
Shanghai
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jun Pu
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Alpha-Ketoglutarate and Abdominal Aortic Aneurysm Progression and Rupture
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