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Nutritional intervention of dietary protocatechuic acid in people with hypercholesterolemia

Nutritional intervention of dietary protocatechuic acid in people with hypercholesterolemia

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067756
Enrollment
Unknown
Registered
2023-01-20
Start date
2022-11-01
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Hypercholesterolemia

Interventions

Intervention group:Protocatechuic acid capsules for three months, one capsule per day
Control group:Placebo capsules for three months, one capsule per day

Sponsors

Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age between 35-65 years old, BMI: 24-30kg/m^2, permanent resident of Guangzhou City (those who have lived in Guangzhou for more than 10 years); 2. The concentration of total cholesterol in fasting blood was between 200-310 mg/dL (5.2-8.0 mmol/L); 3. The smoking index is less than 400 years (smoking index = number of cigarettes smoked per day x smoking years); 4. Weekly alcohol consumption is less than 175g of alcohol; 5. The cumulative time of weekly high-intensity exercise does not exceed 75 minutes or the cumulative time of moderate-intensity exercise does not exceed 150 minutes; 6. Voluntarily participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Have a serious chronic disease that may affect this trial, such as tumors, chronic heart failure, severe depression or other mental disorders, physical disabilities or inability to move freely; 2. Currently taking or having taken any drugs that affect blood lipids and blood sugar in the past six months; 3. Patients with poor compliance; 4. Have suffered from acute and chronic infectious diseases, autoimmune diseases, malignant tumors, trauma or surgery within one month before the test.

Design outcomes

Primary

MeasureTime frame
Flow-mediated dilation function measured by color Doppler ultrasonography;

Secondary

MeasureTime frame
Height;Weight;Waist circumference;Hip circumference;Body fat percentage;Blood pressure;Heart rate;Blood lipids (total cholesterol, triglycerides, high-density lipoprotein cholesterol and low-density lipoprotein cholesterol);Kidney function (creatinine, uric acid, urea nitrogen);Liver function (glutamic-pyruvic transaminase, glutamic oxalacetic transaminase);Blood glucose;Insulin;Bilirubin;Hemoglobin;HDL anti-atherosclerotic function (antioxidant and cholesterol efflux);Serum cytokines adiponectin, leptin, TNF-a, IL-1ß and IL-6;Serum superoxide dismutase;Serum glutathione peroxidase;Malondialdehyde content;Protocatechuic acid content in blood, urine and stool;

Countries

China

Contacts

Public ContactDongliang Wang

Sun Yat-sen University

wdliang@mail.sysu.edu.cn+86 188 1915 4596

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026