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Evaluation of the consumption of grains-based beverage containing functional compounds from purple waxy corn on inflammations in middle-aged and elderly volunteers.

Evaluation of the consumption of grains-based beverage containing functional compounds from purple waxy corn on inflammations in middle-aged and elderly volunteers.

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20221013002
Enrollment
75
Registered
2022-10-13
Start date
2023-02-23
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Healthy condition Purple waxy corn functional beverage anthocyanin dietary fiber

Interventions

Subjects received the placebo product which has the same color and smell and looks like grains-based beverages containing functional compounds.,Subjects received grains-based beverages containing func
Placebo,Grains-based beverage containing functional compounds 2 g/day,Grains-based beverage containing functional compounds 4 g/day

Sponsors

National Research Council of Thailand (NRCT)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 45-65 years old 2. All volunteers don't have cardiovascular diseases or lung disease 3. All volunteers don't get medicine such as anti-inflammatory agents, beta 2-agonists, or other supplements before the start of the test.

Exclusion criteria

Exclusion criteria: 1. Volunteers who have been diagnosed with one of the following; allergies, liver disease, kidney disease, and head injury 2. Drinking alcohol more than 5 times/day 3. Smoking more than 10 pieces/day 4. Volunteers who have regular exercise more than 3 times/week 5. Volunteers who participate in other projects

Design outcomes

Primary

MeasureTime frame
Tumor necrosis factor-alpha 2 months ELISA method

Secondary

MeasureTime frame
Evaluation of Inflammatory markers (IL-4, IL-6, IL-10, IL 1 beta, and C-reactive protein) 2 months ELISA method,Evaluation of Immune markers (CD4, CD8, and CD4+/CD8+ T cell ratio) 2 months ELISA method,Evaluation of Oxidative stress markers; MDA, SOD, CAT, GSH-Px, Nrf2, 8-OHDG, and Sirtuin-1 2 months ELISA method,Evaluation of Neurotransmitters; Acetylcholinesterase and Monoamine oxidase activity 2 months laboratory,Evaluation of Metabolic profiles; Insulin, HbA1C, and HOMA-IR 2 months laboratory,Evaluation of Epigenetic markers; HAT, HDAC, and DNMT1 2 months laboratory,Evaluation of Genetic polymorphism; CYP3A4, CYP3A5*3, and Arc 2 months laboratory,Stool examination; PH, Lactic acid-producing bacteria, Lactobacillus spp., Bifidobacterium spp., and Short chain fatty acid 2 months laboratory,Evaluation of Dynamic lung function; FVC, FEV1, and FEV1/FVC 2 months equipment,The changes of Event-Related Potentials (ERPs) and Computerized battery test 2 months equipment,The changes of Electrocardiogram 2 months Electrocardiography,The changes of hematological and clinical chemistry parameters 2 months laboratory

Countries

Thailand

Contacts

Public ContactJintanaporn Wattanathorn

Faculty of Medicine, Khon Kaen University

jinwat@kku.ac.th66818721909

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026