Keratoconus Clinical Trial
Official title:
The Role of Antioxidants in Keratoconus Patients-A Randomized Controlled Trial of Oral Supplementation of Glutathione, Vitamin A, Vitamin C and Vitamin E
NCT number | NCT02827747 |
Other study ID # | 20150646 |
Secondary ID | |
Status | Withdrawn |
Phase | Phase 2 |
First received | |
Last updated | |
Start date | August 1, 2021 |
Est. completion date | March 2023 |
Verified date | August 2021 |
Source | University of Miami |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Keratoconus is the most common primary cornea ectasia, where the cornea undergoes structural changes, leading to loss of tissue integrity and vision loss. The prevalence of Keratoconus is 1:2000 in the general population. Oxidative stress has been thought to have a major effect in the disease pathogenesis of Keratoconus. In vitro studies have shown increase in metabolites related to oxidative stress in Keratoconus disease, and that Keratoconus cells undergo increased oxidative stress and tissue damage. Animal models have shown a therapeutic effect of Vitamin C (ascorbate) in corneal wound healing. Glutathione and Vitamins A, C, and E are important antioxidants in the human body. To this date, the role of systemic antioxidant supplementation in Keratoconus patients has yet to be studied. In addition, it has yet to be established as to whether there is a correlation between serum antioxidant levels, and the severity of disease in the Keratoconus patient. The investigators propose to investigate the plasma levels of antioxidants in relation to disease severity. The investigators will also investigate the role of antioxidant supplementation-consisting of parenteral Glutathione (GSH), and Vitamins A, C and E-in delaying the disease progression in Keratoconus.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | March 2023 |
Est. primary completion date | July 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 45 Years |
Eligibility | Inclusion Criteria: - Participants would be without illness or condition that could make follow-up, or compliance with study medication difficult. - Participants may have a prior diagnosis of Keratoconus, or may be diagnosed at the initial visit. - Participants should not have an eye diagnosis, other than Keratoconus, that could adversely influence the visual acuity. - These participants must not have had prior surgical procedure to treat Keratoconus, including collagen cross-linking, Intacs ring segments, or corneal transplantation. Exclusion Criteria: - would exclude smokers and former-smokers. |
Country | Name | City | State |
---|---|---|---|
United States | Bascom Palmer Eye Institute-- Palm Beach Gardens | Palm Beach Gardens | Florida |
Lead Sponsor | Collaborator |
---|---|
University of Miami | Fight for Sight |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Visual Acuity Measured by Snellen Chart | Baseline to 24 months | ||
Secondary | Change in cornea thickness as measured by video keratography | Baseline to 24 months | ||
Secondary | Plasma level of Vitamin A | Blood draws to look at plasma level of Vitamin A | Baseline to 24 months | |
Secondary | Plasma level of Vitamin C | Blood draws to look at plasma level of Vitamin C | Baseline to 24 months | |
Secondary | Plasma level of Vitamin E | Blood draws to look at plasma level of Vitamin E | Baseline to 24 months | |
Secondary | Plasma level of Glutathione (GSH) | Blood draws to look at plasma level of GSH | Baseline to 24 months |
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