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Clinical Trial for Nutrilite Vision Health Product

The Effect of Botanical Formula Containing Lutein Ester and Zeaxanthin on Adults with Eye Fatigue in a Double-Blinded, Placebo-Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018987
Enrollment
Unknown
Registered
2018-10-20
Start date
2018-10-20
Completion date
Unknown
Last updated
2020-02-03

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

Conditions

Eye Fatigue

Interventions

Low Dose of LEZ Group:orally receive LEZ containg 6 mg of lutein once daily
Midium Dose of LEZ Group:orally receive LEZ containg 10 mg of lutein once daily
High Dose of LEZ Group:orally receive LEZ containg 14 mg of lutein once daily
Placebo Group:orally receive placebo once daily

Sponsors

Xin Hua Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 65 years; 2. Do extended near work each day with eye strain or tired eyes; 3. Signed informed consent obtained for participating the study.

Exclusion criteria

Exclusion criteria: 1. Subject has infectious or traumatic eye diseases or had an eye surgery within 3 months; 2. Subject has either internal or external eye diseases with cornea, lens, vitreous body, and fundus lesions, and etc.; 3. Subject has disease of cardiovascular, cerebrovascular, liver, kidney, hematopoietic system and other diseases; 4. Subject is pregnant or lactating, or has an allergy; 5. Subject currently takes any drugs or food supplement related to the study product in recent days, which interferes with the study product; 6. Subject currently takes drugs, nutrition supplements or on any therapy for the treatment of eye disease for a long period of time and not willing to discontinue them; 7. Subject participated another clinical trial in the past three months; 8. Subject is not willing to comply the study procedures; 9. Subject has any diseases that can affect the evaluation of the study product; 10. Subject takes any drugs that can affect the evaluation of the study product.

Design outcomes

Primary

MeasureTime frame
Macular Pigment Optical Density;Visual Fatigue Symptom Evaluation;Visuognosis Persistence;Schirmer test;

Secondary

MeasureTime frame
Vision test;Optical Coherence Tomography;Body composition analysis;Food frequency questionnaire;Routine blood test;Urinalysis;Kidney function test;Liver function test;Blood lipid profile;

Countries

China

Contacts

Public ContactJuntao Kan

Amway (China) R&D Center

junot.kan@amway.com+86 13585657829

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 26, 2026