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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03630328
Other study ID # STUDY00008009
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date February 6, 2019
Est. completion date December 2025

Study information

Verified date February 2024
Source Milton S. Hershey Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This human study will test the impact of dietary supplement vegicaps containing Korean Angelica root extract on 2 types of human immune cells: neutrophils that kill bacteria and other germs and natural killer (NK) cells that kill virus-infected cells and cancers. The investigators had done an earlier study with Korean Angelica supplement and discovered even a single dose of it increased blood neutrophils and NK cells within 24 h. In the new study, Korean Angelica capsules (Cogni.Q) will be compared head-to-head with dummy (placebo) capsules. This is to make sure the immune boosting actions are really from the Korean Angelica supplement.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 40
Est. completion date December 2025
Est. primary completion date August 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 21 Years to 65 Years
Eligibility Inclusion Criteria: - Subjects weighing between 110 to 240 pounds; their body mass index (BMI) should be in the range of 19 to 30 - Subjects having normal hepatic, renal function as assessed by history, physical and clinical chemistry analysis (CMP eGFR, see supporting document for normal reference ranges). - Subjects with normal blood pressure (systolic below 120 mm Hg and diastolic below 80 mm Hg) Exclusion Criteria: - Subjects positive for HIV, HBV and HCV (self-reported) - Subjects taking any kind of prescription medications regularly or within 10 days of the study will be excluded. Therefore, subjects with diabetes, major cardiovascular diseases, cancer, severe hypertension, severe hepatic cirrhosis or cirrhosis of the liver, and kidney disease (self-reported) will be excluded. - Subjects using tobacco products, nicotine patches and excessive alcohol - Subjects taking dietary or herbal supplements that contain AGN (e.g. Cogni.Q, Decursinol-50, Ache Action, Fast-Acting Joint Formula, EstroG-100/Profemin) within 10 days of the study. - Non-English-speaking subjects

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Cogni.Q
AGN
Other:
Placebo
Placebo

Locations

Country Name City State
United States Penn State College of Medicine Hershey Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Milton S. Hershey Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Neutrophil counts and NK cell counts in peripheral blood Using CBC diff to measure neutrophil counts, NK cells number will be enumerated using flowcytometer 70 days
Secondary T cells in peripheral blood, T cells number will be enumerated using flowcytometer 70 days
Secondary Plasma concentrations of pyranocoumarins, androgens, and inflammatory/anti-inflammatory cytokines. Determine Plasma concentrations of pyranocoumarins (as compliance marker), androgens, and inflammatory/anti-inflammatory cytokines. 70 days
Secondary Lipid profiling blood test will be done at every visit 70 days
Secondary NK mRNA signature NK mRNA signature by RNA-seq transcriptomics using RNA prepared from Pax Gene tube-preserved whole blood collected on each visit 70 days
Secondary PBMC isolation for testing NK activity PBMCs will be isolated at every blood draw and kept frozen. They will be used to determine NK cell activity in future. 70 days
Secondary CMP-EGFR blood test will be done at every visit 70 days