Skip to content

A human experimental study on the effect of Thomson Beijian Xinluosu Tablets on platelet aggregation function

A human experimental study on the effect of Thomson Beijian Xinluosu Tablets on platelet aggregation function

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054361
Enrollment
Unknown
Registered
2021-12-15
Start date
2021-06-16
Completion date
Unknown
Last updated
2022-11-20

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

Conditions

cardiovascular diseases

Interventions

Control group:Placebo
Experimental group:Xinluosu Tablets

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 35 to 65 years, gender is not limited; 2. No obvious vascular or blood system diseases; 3. No abnormality in laboratory tests: blood routine, liver and kidney function, blood sugar, blood lipids, coagulation function, etc.; 4. Healthy volunteers who signed informed consent and volunteered to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Currently taking any medication; 2. Low platelet count (whole blood <100 x 10^9/L); 3. Prothrombin time (PT) is outside the normal reference range; 4. Receive chronic medication and nutritional supplements; 5. Pregnant or breastfeeding; 6. According to the judgment of the investigator, there is a history of the following related diseases: digestive system diseases, organic diseases of the heart, liver or kidney, severe liver or kidney dysfunction, metabolic/endocrine/nervous system diseases, Neurological disorders (eg, Parkinson's disease, stroke) with residual damage, vertigo; 7. Abnormal menstrual cycle, taking contraceptives or hormone replacement therapy; or women in menopause; 8. Persons who are not suitable for venous blood collection; 9. Allergic to tomato and its components; 10. Known HIV history or active HCV/HBV infection or uncontrolled active systemic infection; 11. Have participated in or are participating in other clinical trials within three months of taking the research product for the first time; 12. Those who take fish oil and evening primrose; 13. Supplement functional foods, supplements and drugs that affect platelet function; 14. Those who cannot tolerate or are allergic to aspirin or those who are in line with the contraindication of aspirin.

Design outcomes

Primary

MeasureTime frame
platelet aggregation ratio;blood routine examination;liver function test;Renal function test;

Countries

China

Contacts

Public ContactQi Ruomei

Beijing Hospital

ruomeiqi@163.com+86 10 58115047

Outcome results

None listed

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