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Human intervention study on dietary intake of water-soluble tomato extract

Human intervention study on dietary intake of water-soluble tomato extract: a randomized, cross-over clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-POR-17012927
Enrollment
Unknown
Registered
2017-10-10
Start date
2017-10-20
Completion date
Unknown
Last updated
2020-03-09

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

Conditions

healthy

Interventions

water-soluble tomato extract group:take orally 300 mg drug per day(contains 150mg water-soluble tomato extract )
placebo group:take orally 300 mg placebo per day

Sponsors

School of Public Health, Sun YatSen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. aged 35-70 years old, males or females; 2. with no medical history of serious disease, haemostatic disorders.

Exclusion criteria

Exclusion criteria: 1. consuming drugs known to affect platelet function for a 2-week period prior to participation; 2. pregnant or lactating women; 3. mental abnormality; 4. allergic to the components of the supplement used in this test.

Design outcomes

Primary

MeasureTime frame
platelet aggregation;p-selectin;—

Secondary

MeasureTime frame
Coagulation function;—

Countries

China

Contacts

Public ContactYang Yan

School of Public Health, Sun YatSen University

yangyan3@mail.sysu.edu.cn+86 020-87330687

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026