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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03865745
Other study ID # GINGAM
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 2019
Est. completion date February 2020

Study information

Verified date March 2019
Source MedicalExcellence
Contact Youn Ju Lee
Phone 82-2-3482-7834
Email yj.lee@mediex.co.kr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the positive effects of red ginseng extract on intestinal bacterial changes and immunity, free radicals, antioxidant capacity, and autonomic nervous system changes in age of 40~75 men and women with climacteric symptoms for 24 weeks.


Description:

A screening test is conducted for those who have agreed in writing with a detailed explanation of the purpose of this study and research methods, and then a person who meets the selection / exclusion criteria is selected.

Give a registration number to the person selected as the subject through the screening, and take one pack of the product (3g) once a day for 24 weeks in a human body application test.

Prior to taking the registration number (1Day), the efficacy evaluation items and the safety evaluation items are carried out. At the 24 weeks after the starting point of taking the product of human application test, the evaluation items are conducted through outpatient visits.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 53
Est. completion date February 2020
Est. primary completion date February 2020
Accepts healthy volunteers No
Gender All
Age group 40 Years to 75 Years
Eligibility Inclusion Criteria:

1. Age of 40~75 men and women

2. Those who visited the menopausal clinic with complaints of climacteric symptoms due to functional deterioration of various organs such as fatigue, helplessness

3. Those who have agreed to voluntarily decide to participate and observe the instructions after hearing the detailed explanation of this human body application test

Exclusion Criteria:

1. Those who have suspected symptoms of acute disease (severe infectious disease, severe trauma, severe diarrhea, vomiting, etc.)

2. Patients with a history of antibiotic treatment for more than 1 month within the last 6 months

3. Those who have gastrointestinal diseases (inflammatory growth disease, active peptic ulcer, etc.) or gastrointestinal surgery (except for simple appendectomy or hernia surgery)

4. Those taking health functional foods, lactic acid bacteria, and red ginseng extracts for the past year

5. Those who are currently participating in other clinical studies or human trials, or participating in clinical trials or human application tests within the past month

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Korean Red Ginseng
Take one pack of the product (3g) once a day for 24 weeks

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
MedicalExcellence

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in gut microbiota at 24 weeks vs baseline 24 weeks
Secondary Changes in Total Oxidant Status(TOS in µmol/L) at 24 weeks vs baseline 24 weeks
Secondary Changes in Total Antioxidant Status(TAS in mmol/L) at 24 weeks vs baseline 24 weeks
Secondary Changes in Natural Killer(NK) cell activity at 24 weeks vs baseline 24 weeks
Secondary Changes in Heart rate variability at 24 weeks vs baseline 24 weeks
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