Immunity Clinical Trial
Verified date | August 2019 |
Source | Chonbuk National University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators performed a 12-week, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of Cauliflower Mushroom extract on promotion of immunity. The investigators measured promotion of immunity parameters , including Cytotoxicity, Cytokine (IL-4, IL-10, IFN- γ, TNF-α), and CBC (WBC, RBC, Hb, Hct, MCV, MCH, MCHC, PLT), and monitored their blood pressure.
Status | Completed |
Enrollment | 60 |
Est. completion date | January 18, 2013 |
Est. primary completion date | January 18, 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 30 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Males and females 30-65 years old - Weight within ±30% of ideal body weight - Able to give informed consent Exclusion Criteria: - WBC concentration below 3000 ? - Allergic or hypersensitive to any of the ingredients in the test products - Diagnosed of gastrointestinal disease such as Immune-related diseases, severe hepatic, renal failure, and diabetes - History of reaction to any of the test products or of gastrointestinal diseases such as Crohn's disease or gastrointestinal surgery - History of alcohol or substance abuse - Participation in any other clinical trials within past 2 months - Laboratory test, medical or psychological conditions deemed by the investigators to interfere with successful participation in the study - Pregnant or lactating women etc. |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Clinical Trial Center for Functional Foods; Chonbuk National University Hospital | Jeonju | Jeollabuk-do |
Lead Sponsor | Collaborator |
---|---|
Chonbuk National University Hospital |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in Cytotoxicity | Cytotoxicity was measured in study visit 1(0 week) and visit 3(12 week). cytotoxicity was measured by NK cell activity. Cytotoxicity (%) = (experimental release - spontaneous release) / (maximum release - spontaneous release) x 100 | 12 weeks | |
Primary | Changes in Cytokine (IL-4, IL-10, IFN- ?, TNF-a) | Cytokine (IL-4, IL-10, IFN- ?, TNF-a) was measured in study visit 1(0 week) and visit 3(12 week). | 12 weeks | |
Secondary | Changes in CBC (WBC, RBC, Hb, Hct, MCV, MCH, MCHC, PLT) | CBC (WBC, RBC, Hb, Hct, MCV, MCH, MCHC, PLT) was measured in study visit 1(0 week) and visit 3(12 week). | 12 weeks |
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