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Supplement intake test

Not Applicable
Conditions
Glaucoma, Cataract, Diabetic retinopathy, central serous chorioretinopathy
Registration Number
JPRN-jRCTs021180019
Lead Sponsor
Himori Noriko
Brief Summary

Our study found that an 8-week oral course of antioxidant supplementation was effective. Dietary supplementation holds promise in the treatment of systemic oxidative stress-related diseases.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
53
Inclusion Criteria

1.Patients with glaucoma, cataract, diabetic retinopathy, central serous chorioretinopathy
2.Glaucoma stage: Normal tension glaucoma(in medical treatment eye intraocular pressure less than 16mmHg)
Cataract:Nuclear cataract
Diabetic retinopathy:simple or non proliferative
Central serous chorioretinopathy:all
3.Age:more than 30 years old, less than 75 years old (at entry)
4.BAP:more than 1600umol/L, less than 2200 umol/L
5.dROMs:more than 300CARR
6.BMI:less than 26kg/m2

Exclusion Criteria

1.Other ophthalmic condition in hospital
2.High myopia
3.LASIK
4.After ophthalmic surgery within three months
5.Cancer patient
6.Autoimmune disease
7.Take a pill
8.other supplements intake
9.other clinical trial
10.allergy
11.pregnant, breast-feeding
12.Patient judged inappropriate by the attending physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Antioxidative potential, BAP level
Secondary Outcome Measures
NameTimeMethod
oxidative stress, dROMs level, 8OHdG level, blood flow of ONH
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