Skip to content

Effect of Aged Garlic Extract on Atherosclerosis

Effect of Aged Garlic Extract on Atherosclerosis

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01534910
Acronym
Garlic4
Enrollment
65
Registered
2012-02-17
Start date
2012-05-31
Completion date
2014-12-31
Last updated
2017-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic Syndrome

Keywords

garlic, ct angiography, atherosclerosis, carotid IMT

Brief summary

The investigators will be assessing the effect of Aged Garlic Extract on the coronary arteries. The investigators will enroll patients in a double blind study, where half the patients will receive placebo, and have the patients undergo a series of tests of plaque (CT scan of the heart, carotid ultrasound) and follow the patients on the drug or placebo and then repeat the tests and blood work at the end of one year. The investigators will assess if being on aged garlic extract adds any benefit to plaque in the coronary or neck arteries. The investigators will also assess the effect of aged garlic extract on markers of inflammation. Patients will receive free drug, free testing and be compensated, and learn more about their heart and neck arteries. if successful, more patients can use this drug to benefit their health. The harms include the radiation from the CT scan and the medication, which has mild side effects.

Detailed description

The investigators will be assessing the effect of Aged Garlic Extract on the coronary arteries. The investigators will enroll patients in a double blind study, where half the patients will receive placebo, and have the patients undergo a series of tests of plaque (CT scan of the heart, carotid ultrasound) and follow the patients on the drug or placebo and then repeat the tests and blood work at the end of one year. The investigators will assess if being on aged garlic extract adds any benefit to plaque in the coronary or neck arteries. The investigators will also assess the effect of aged garlic extract on markers of inflammation. Patients will receive free drug, free testing and be compensated, and learn more about their heart and neck arteries. if successful, more patients can use this drug to benefit their health. The harms include the radiation from the CT scan and the medication, which has mild side effects. The study will perform advanced CT angiography at baseline and follow up along with carotid intimal media thickness testing, to see if plaque is slowed down by Aged Garlic Extract

Interventions

2400 mg a day

DRUGplacebo

placebo

Sponsors

Wakunaga Pharmaceutical Co., Ltd.
CollaboratorINDUSTRY
Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 40-65 years * Framingham risk score 6-20%, and at least 2 components of the metabolic syndrome as defined by ATP III Clinical Identification of the Metabolic Syndrome (including impaired fasting glucose \> 110 mg/dl, treated hypertension or SBP \> 130 or DBP \> 85 mm Hg, plasma triglycerides \> 150 mg/dl, HDL cholesterol \< 35 mg/dl for men or \< 40 mg/dl for women, abdominal obesity as defined as waist \> 40 in for men, \> 35 in for women) * Subjects must provide written informed consent after the scope and nature of the investigation has been explained to them * Subjects should be stable on their concomitant medications for at least 26 weeks prior to randomization * Calcium Score \> 20 at baseline * Subjects who agree to refrain from other anti-glycemic agent

Exclusion criteria

* A contraindication to AGE including: known hypersensitivity to drug. * Any unstable medical, psychiatric or substance abuse disorder that in the opinion of the investigator or principal investigator is likely to affect the subject's ability to complete the study or precludes the subject's participation in the study * Weight in excess of 300 pounds * Bleeding disorder * History of known coronary artery disease, myocardial infarction, stroke or life-threatening arrhythmia within the prior six months * NYHA Class II- IV heart failure * History of malignancy within the last 5 years (other than skin cancer) or evidence of active cancer which would require concomitant cancer chemotherapy * Serum creatinine \> 1.4 mg/dl * Diabetes Mellitus * Triglycerides \> 400 at visit 1 * Drug or alcohol abuse, or current intake of more than 14 standard drinks per week * Concurrent enrollment in another placebo-controlled trial * Partial ileal bypass or known gastrointestinal disease limiting drug absorption * Current diabetes or intake of anti-diabetic or other prohibited drug * Current tobacco use * Current use of anticoagulants (except for anti-platelet agents) * Renal failure * History of hypertensive encephalopathy or cerebrovascular accident * Hematological or biochemical values at screening outside the reference ranges considered as clinically significant in the opinion of the investigator or PI

Design outcomes

Primary

MeasureTime frameDescription
CT Angiography Plaquebaseline to 1 yearwe will measure low attenuation plaque at baseline (in volume) and then again at 1 year. we will assess if there is a reduction in low attenuation plaque volume (percent change from baseline), defined as \[followup-baseline\]/baseline x100%. Baseline was time zero, followup CT scan was 1 year.

Secondary

MeasureTime frameDescription
Coronary Calcium1 yearAgatston score is a semi-automated tool to calculate a score based on the extent of coronary artery calcification detected by an unenhanced low-dose CT scan. The calculation is based on the weighted density score given to the highest attenuation value (HU) multiplied by area of the calcification speck. The grading of coronary artery disease (based on total calcium score) is as follows: no evidence of CAD: 0 calcium score, minimal: 1-10, mild: 11-100, moderate: 101-400, and severe: \>400

Countries

United States

Participant flow

Recruitment details

all 65 participants were recruited

Participants by arm

ArmCount
Sugar Pill
placebo placebo: placebo patients were randomized to placebo
33
Aged Garlic Extract
2400 mg of aged garlic extract aged garlic extract: 2400 mg a day patients randomized to aged garlic extract
32
Total65

Baseline characteristics

CharacteristicAged Garlic ExtractSugar PillTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
32 Participants33 Participants65 Participants
Age, Continuous56 years
STANDARD_DEVIATION 8
57 years
STANDARD_DEVIATION 7
57 years
STANDARD_DEVIATION 7
Region of Enrollment
United States
32 participants33 participants65 participants
Sex: Female, Male
Female
8 Participants9 Participants17 Participants
Sex: Female, Male
Male
24 Participants24 Participants48 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 330 / 32
serious
Total, serious adverse events
0 / 330 / 32

Outcome results

Primary

CT Angiography Plaque

we will measure low attenuation plaque at baseline (in volume) and then again at 1 year. we will assess if there is a reduction in low attenuation plaque volume (percent change from baseline), defined as \[followup-baseline\]/baseline x100%. Baseline was time zero, followup CT scan was 1 year.

Time frame: baseline to 1 year

ArmMeasureValue (MEAN)Dispersion
Sugar PillCT Angiography Plaque0.17 percent change of low attenuation plaqueStandard Deviation 1.97
Aged Garlic ExtractCT Angiography Plaque-1.53 percent change of low attenuation plaqueStandard Deviation 2.32
Secondary

Coronary Calcium

Agatston score is a semi-automated tool to calculate a score based on the extent of coronary artery calcification detected by an unenhanced low-dose CT scan. The calculation is based on the weighted density score given to the highest attenuation value (HU) multiplied by area of the calcification speck. The grading of coronary artery disease (based on total calcium score) is as follows: no evidence of CAD: 0 calcium score, minimal: 1-10, mild: 11-100, moderate: 101-400, and severe: \>400

Time frame: 1 year

Population: patients undergoing two calcium scores

ArmMeasureValue (MEAN)
Sugar PillCoronary Calcium95 agatston units
Aged Garlic ExtractCoronary Calcium49 agatston units

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026