Aged Garlic Extract Study
Launched by LUND UNIVERSITY HOSPITAL · Feb 28, 2019
Trial Information
Current as of May 21, 2025
Completed
Keywords
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Lund, , Sweden
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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