Efficacy and Safety of Hydrolysed Red Ginseng Extract on Dry Eye

Dry Eye Clinical Trial

Official title:

A 12 Weeks, Randomized, Double-blind, Placebo-controlled Human Trial to Evaluate the Efficacy and Safety of Hydrolysed Red Ginseng Extract on Dry Eye

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03992287
• Other study ID #: GH-DE-HR
• Status: Recruiting
• Phase: N/A
• Start date: March 1, 2019
• Est. completion date: July 31, 2020

Study information

• Verified date: November 2019
• Source: Chonbuk National University Hospital
• Contact: In Cheon You, M.D., Ph.D.
• Phone: +82-63-250-258
• Email: you2ic[@]jbnu.ac.kr
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study was conducted to investigate the effects of daily supplementation of Hydrolysed Red Ginseng Extract extract on dry eye.

Description:

This study was a 12 weeks, randomized, double-blind, placebo-controlled human trial. 46 subjects were randomly divided into Hydrolysed Red Ginseng extract 10ml or placebo group. The investigators measured Ocular Surface Disease Index, tear break-up time, Visual analog scale, Schirmer's test, meibomian gland test and Fluorescein staining.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 46
• Est. completion date: July 31, 2020
• Est. primary completion date: March 30, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 19 Years and older

Eligibility

Inclusion Criteria:

• Adult men and women over 19years

• Ocular Surface Disease Index score is 13 scores and more at a screening

• Tear Break-Up Time is 10 seconds less or those who have positive in ocular staining test at a screening

• After fully hearing and fully understanding this clinical trials, those who agree to voluntarily decide to participate and to comply with the notice

Exclusion Criteria:

• Those who have a body mass index(BMI) of less than 18.5 kg / m^2 or greater than 35 kg / m^2 at the screening

• Those who have clinically significant acute or chronic ophthalmologic, cardiovascular system, endocrine, immune, respiratory, liver biliary system, renal and urinary tract, neuropsychiatry, musculoskeletal, inflammatory and hematologic and gastrointestinal disorders

• Those who couldn't control diabetes at screening

• Those with acute eye infections or inflammation within 1 month before screening

• Those who have ophthalmic surgery within 3 months before screening

• Those who use contact lens 1 month before screening

• Those who take a medication or health function food that affects your promotion of dry eye within 1 month prior to the screening

• Those who have received antipsychotic medication within 3 months before screening

• Those who alcoholic or drug abuse suspected

• Those who participated in other clinical trials within 3 months before screening

• Laboratory test by showing the following results

• Aspartate Transaminase(AST), Alanine Transaminase(ALT) > Reference range 3 times upper limit

• Serum Creatinine > 2.0 mg/dL

• Pregnancy or breastfeeding

• Those who don't accept the implementation of appropriate contraception of a childbearing woman

• Principal Investigator judged inappropriate for participation in the study because of Laboratory test results, etc.

Related Conditions & MeSH terms

• Dry Eye
• Dry Eye Syndromes
• Keratoconjunctivitis Sicca

Intervention

Dietary Supplement:
• Hydrolysed Red Ginseng Extract
10 ml/day, 2.4g/day for 12 weeks
• Placebo
Placebo for 12 weeks

Locations

Country	Name	City	State
Korea, Republic of	Clinical Trial Center for Functional Foods Chonbuk National University Hospital	Jeonju	Jeollabuk-do

Sponsors (1)

Lead Sponsor	Collaborator
Chonbuk National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes of Ocular Surface Disease Index	A questionnaire which is Ocular Surface Disease Index consisted of 12 questions each of which included visual symptoms, visual work status, and environmental factors.; The Ocular Surface Disease Index scores are ranged from 0 to 100, and the high score is the more severe the symptoms. The Ocular Surface Disease Index score is calculated as follows.; : (Sum of all items answered × 25) / total number of questions answered	12 weeks
Primary	Changes of tear break-up time	The tear break-up time test measures the time in seconds. The time is from the last blinking to the point of tear layer defect or streak-like defect after blinking the eye with 1% of fluorescein.; 10 seconds or more as normal, between 5 and 10 seconds as mild dry eye syndrome, and 5 seconds or less as severe dry eye syndrome.	12 weeks
Secondary	Changes of Visual analog scale	The Visual Analog Scale(VAS) score is 0 point for no symptom, 10 points for the most severe symptom, and the patient is asked to mark the degree of subjective pain symptoms as an integer.	12 weeks
Secondary	Changes of Schirmer's test	Schirmer's test determines whether the eye produces enough tears to keep it moist. This test is used when a person experiences very dry eyes or excessive watering of the eyes. It poses no risk to the subject. A negative (more than 10 mm of moisture on the filter paper in 5 minutes) test result is normal. Both eyes normally secrete the same amount of tears.	12 weeks
Secondary	Changes of meibomian gland test	Meibomian gland test evaluate 8 Meibum of the upper middle eyelid or lower middle eyelid. The Meibum quality score and the Meibum expressibility score are evaluated as follows.; Meibum quality score 0 = clear fluid; = cloudy fluid; = cloudy particulate fluid(with debris); = inspissated (opaque),like toothpaste; Meibum expressibility score 0 = all glands expressible; = three to four glands expressible; = one to two glands expressible; = no glands expressible	12 weeks
Secondary	Changes of Fluorescein staining	Fluorescein staining was evaluated by staining with 1% fluorescein (1% sodium fluorescein 1 µL volume), and then assessed for damage after corneal and conjunctival staining. The degree of staining of the cornea is divided into 5 sections according to the NEI scale, and each section is judged as 0 ~ 3 scores. It is judgement the degree of severity from 0 to 15 scores per eye. The degree of conjunctival staining is divided into six sections per eye, and each section is scored 0 to 3 scores total 0 ~ 18 scores.	12 weeks