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Effects of Lactobacillus plantarum supplementation on lipid profiles among Chinese with mild dyslipidemia

Effects of Lactobacillus plantarum on lipid profile

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058631
Enrollment
Unknown
Registered
2022-04-12
Start date
2022-04-11
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Dyslipidemia

Interventions

Intervention group:Lactobacillus plantarum granules , once a day, 1 bag (1 g) each time (contains 1.2 billion cfu of viable bacteria), take with warm water (less than 37 degrees), lifestyle guidance
Control group:Placebo (maltodextrin) gradules, once a day, 1 bag (1 g)each time, take with warm water (less than 37 degrees), lifestyle guidance.

Sponsors

Xi’an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-70 years; 2. 3.4 = LDL-C<4.9 mmol/L, 5.18 = TC<7.2 mmol/L, and 1.7 = TG<5.6 mmol/L; 3. They did not use lipid-lowering drugs, or they took lipid-lowering drugs and stopped taking them for more than 3 months.

Exclusion criteria

Exclusion criteria: 1. Those who cannot eat by mouth or take the test sample as required; 2. The principal complaint is unclear; 3. Pregnant or lactating women, pregnant women; 4. Allergic constitution or allergy to the test sample; 5. ASCVD risk is assessed as high risk (ASCVD risk is assessed according to the assessment form of Guidelines for the Prevention and Treatment of Dyslipidemia in Chinese Adults (2016 Revision)) *; 6. Those who have undergone digestive system surgery within 30 days are currently or within 30 days receiving antibiotic treatment (except for skin or reproductive tract drugs); 7. Inpatients or those with acute gastrointestinal diseases within 2 weeks; 8. Patients with serious diseases and mental disorders such as heart, liver, kidney and hematopoietic system; 9. Those who regularly take probiotic products within 30 days, and have taken drugs (including but not limited to phytosterol, berberine, Monacolin K) that affect blood lipid within 2 weeks, affect the judgment of the results; 10. Abnormal liver and kidney function; Suffering from diseases that affect blood lipid metabolism (including but not limited to thyroid diseases, biliary diseases, pancreatitis and immune disorders); Severe hyperacidity (including but not limited to regular administration of H2 receptor blockers, proton pump inhibitors and other antacid drugs within 2 weeks); Severe constipation (including but not limited to regular use of laxatives such as loperamide within 2 weeks); 11. Those who fail to take interventions as required during the induction period and cannot comply; 12. Less than 30 years old and there is evidence that there is a tendency of hereditary hyperlipidemia; 13. Other patients considered by the investigator not suitable for the study; 14. Those who do not sign the informed consent form.

Design outcomes

Secondary

MeasureTime frame
Serum total cholesterol (TC);High-density lipoprotein cholesterol (HDL-C);Triglycerides (TG);Glucose;Insulin;BMI;The diversity and abundance of intestinal flora (16S);

Primary

MeasureTime frame
Serum Low Density Lipoprotein Cholesterol (LDL-C);

Countries

China

Contacts

Public ContactXin Lin

Xi’an Jiaotong University

xinliu@xjtu.edu.cn+86 15009202712

Outcome results

None listed

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