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Completed

NCT Number: NCT03860350

Aged Garlic Extract Study

The primary intention of the study is to examine the effect of aged garlic extract (AGE) on the absolute change in coronary artery calcium (CAC). The second intention is to examine the effect of AGE on inflammatory biomarkers and microcirculation. It is a double blind placebo controlled study. The participants will ingest AGE during a period of one year. The CAC will be controlled by computer tomography (CT) scan; the inflammatory biomarkers through blood sample test and the microcirculation through laser speckel imagining and laser doppler before and after the one year period of AGE ingestion.

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Key information

Age range

40 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Skane University Hospital

Lund, 22241, Sweden

About this study

Objectives:

Effect on coronary artery atherosclerosis / the progression of atherosclerosis Effect on inflammatory and oxidation biomarkers Cholesterol lowering effect Effect on microcirculation

Type of study:

Randomized double blind controlled trial

Number of patients: 80 patients

Duration of the study:

The patients will be studied for one year after they have entered the study. The total time of the study duration from the including date of the first patient to the analysis of the last patient entering the study estimated to be 2-3 years. An inclusion rate off 1 to 2 patients per week.

Treatment:

Dose: Treated with a placebo capsule or a capsule containing a total of AGE 2400 mg daily for 1 year (2 Kyolic capsule (600 mg) twice daily).

Methods:

Placebo-controlled double blind randomized trial to determine whether AGE can influence the rate of atherosclerosis plaque burden measured by coronary artery calcium, improve vascular function and microcirculation and favorably change biomarkers of oxidative stress.

Randomization:

The participants are assigned to AGE or placebo in a double-blinded manner, using numbered containers assigned to a computer-generated randomization chart by a nurse coordinator.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • CAC score >10
  • Framingham risk score (10 % or above)
  • Subjects are required to be on stable concomitant medications for at least 12 weeks prior to randomization
  • Subjects with diabetic must have HbA1C < 8.0, and stable HbA1C level variation range within 0.5% for three months.

Exclusion criteria

  • Hypersensitivity to AGE therapy,
  • Unstable medical, psychiatric, or substance abuse disorder that may interfere with continuation in the study,
  • Weight ≥325 pounds,
  • Bleeding disorder,
  • History of myocardial infarction,
  • Stroke
  • Life-threatening arrhythmia within prior 6 months,
  • Resting hypotension (systolic < 90 mmHg) or hypertension (resting blood pressure >170/110)
  • Heart failure NYHA class III or IV,
  • 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
  • Triglycerides > 400 at baseline visit
  • Diabetic subjects with HbA1C > 8 %,
  • Drug or alcohol abuse
  • Conditions interfering with accurate assessment of coronary calcification (metal clips, bypass patients, intracoronary stents) and drug absorption (partial ileal bypass or malabsorption syndrome).
  • Current use of anticoagulants (except for antiplatelet agents)
  • Chronic renal failure
  • Liver failure
  • Hematological or biochemical values at baseline visit outside the reference ranges considered as clinically significant.

Treatment and study plan

Aged Garlic Extract

Dietary Supplement

Other names: Kyolic

Placebo

Dietary Supplement

Primary outcomes

  1. Change in coronary artery calcium (CAC) score

    Time frame: One year

    CAC is to be defined as a plaque of at least three contiguous pixels (area 1.02 mm 2) with a density of > 130 Hounsfield units. The lesion score are to be calculated by multiplying the lesion area by a density factor derived from the maximal Hounsfield unit within this area, as described by Agatston S, Janowitz WR, Hildner FJ et al. Quantification of coronary artery calcium using ultrafast computed tomography. J Am Coll Cardiol 1990; 15: 827-832. CAC score is measured at baseline and after one year follow-up and the difference is calculated.

Secondary outcomes

  1. The changes in inflammatory biomarkers.

    Time frame: One Year

    Changes in C-reactive protein (CRP mg/L)

  2. The changes in Interleukin-6 (IL-6)

    Time frame: One Year

    Changes in IL-6 (ng/L)

  3. The changes in inflammatory biomarkers.

    Time frame: One Year

    Changes in Homocystein (µmol/L)

  4. The changes in the microcirculation measured by Laser Doppler velocimetry

    Time frame: One Year

    Laser Doppler Flowmetry (LDF) is a non-invasive method to estimate the blood perfusion in the microcirculation. The advantage of the technique is that LDF provide a continuous or near continuous record of the microvascular blood flow. No current laser Doppler instrument can present absolute perfusion values (e.g. ml/min/100 gram tissue). Measurements are expressed as perfusion units (PU) which are arbitrary. The changes in PU will be measured.

  5. Changes in Low Density Lipoprotein

    Time frame: One Year

    Changes of Low Density Lipoprotein (LDL) mmol/L

  6. Changes in Triglycerides

    Time frame: One Year

    Changes of Triglycerides mmol/L.

  7. Changes in Cholesterol

    Time frame: One Year

    Changes of cholesterol mmol/L.

  8. Changes in High Density Lipoprotein

    Time frame: One Year

    Changes of High Density Lipoprotein(HDL) mmol/L,

  9. Changes in lipid profile

    Time frame: One Year

    Apolipoprotein B (mmol/L)/Apolipoprotein A1 (mmol/L)

  10. Changes in blood sugar

    Time frame: One Year

    Changes in fastening blood glucose measured as mmol/L

  11. Changes in Blood pressure

    Time frame: One Year

    Changes of blood pressure Systolic and Diastolic presented as mmHg.

  12. Changes in BMI

    Time frame: One Year

    Changes in BMI measured as weight (kg) and height (m) and will be combined to report BMI in kg/m^2

Sponsors and collaborators

Lead sponsor

Lund University Hospital

Other

Registry information

Official study title

Aged Garlic Extract (Kyolic) Study at Lund University, Sweden

Acronym: AGE

Important dates

Study start
2016
Primary completion
2019
Study completion
2019
First posted
Mar 1, 2019
Registry last updated
Jun 11, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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