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Search / Trial NCT03860350

Aged Garlic Extract Study

Launched by LUND UNIVERSITY HOSPITAL · Feb 28, 2019

Trial Information

Current as of May 21, 2025

Completed

Keywords

Garlic

ClinConnect Summary

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 wee...

Gender

ALL

Eligibility criteria

  • 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.

About Lund University Hospital

Lund University Hospital, affiliated with Lund University in Sweden, is a leading institution in medical research and clinical trials. Renowned for its commitment to advancing healthcare through innovative research, the hospital integrates clinical practice with academic excellence. As a sponsor of clinical trials, Lund University Hospital focuses on a wide range of therapeutic areas, striving to improve patient outcomes by rigorously evaluating new treatments and interventions. With a multidisciplinary team of expert researchers and clinicians, the hospital emphasizes ethical standards, patient safety, and scientific integrity in all its studies, contributing significantly to the global medical community.

Locations

Lund, , Sweden

Patients applied

0 patients applied

Trial Officials

Sandra Lindstedt, MD, PhD

Principal Investigator

Skane University Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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