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Dietary Riboflavin (Vitamin B-2) and Cornea Cross-Linking

Primary Purpose

Keratoconus, Cornea Ectasia

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Dietary riboflavin
Sponsored by
University of Missouri-Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Keratoconus focused on measuring keratoconus, cornea ectasia

Eligibility Criteria

12 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • patients identified as having keratoconus or post refractive cornea ectasia with astigmatism of 1.5 Diopters or greater.

Exclusion Criteria:

  • Known sensitivity to riboflavin, sunlight.
  • patients on medications with side effects of increased sunlight sensitivity should discuss participation with their prescribing provider prior to participation

Sites / Locations

  • University of South Florida Department of OphthalmologyRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment with riboflavin

Arm Description

Patients will take 400 mg dietary riboflavin per day and go outside without sunglasses for 15 minutes per day to evaluate the effects of riboflavin B2 and natural UV light from sun exposure on cornea cross linking and stabilization of ectatic disease.

Outcomes

Primary Outcome Measures

Degree of corneal steepening
Keratometry measures the degree of astigmatism of the cornea to monitor the degree of cornea steepening

Secondary Outcome Measures

Best corrected visual acuity
Measures the best vision the patient is able to see at that time

Full Information

First Posted
October 13, 2016
Last Updated
July 26, 2023
Sponsor
University of Missouri-Columbia
Collaborators
University of South Florida
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1. Study Identification

Unique Protocol Identification Number
NCT03095235
Brief Title
Dietary Riboflavin (Vitamin B-2) and Cornea Cross-Linking
Official Title
Dietary Riboflavin (Vitamin B-2) and Cornea Cross-Linking
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2017 (Actual)
Primary Completion Date
January 1, 2024 (Anticipated)
Study Completion Date
January 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Missouri-Columbia
Collaborators
University of South Florida

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Corneal ectasia is characterized by irregularity and thinning of the cornea, causing the cornea to bulge forward and cause distorted vision and impaired visual acuity. Corneal ectasia is a complication after refractive (LASIK) surgery. It is also the primary problem in keratoconus, a gradually progressive inherited condition that typically is manifested in young adulthood, more commonly in women. Treatment approaches to stabilize the cornea's shape include rigid contact lenses, surgical implantation of stiff plastic intrastromal corneal ring segments, a collagen cross-linking procedure and, in severe cases, cornea transplantation. The collagen cross-linking procedure involves topical application of a concentrated riboflavin (vitamin B2) solution after the corneal epithelium is scraped, followed by ultraviolet (UV) light exposure. UV light stimulates riboflavin to form new bonds (cross links) between the cornea's connective tissue, giving the cornea additional strength to maintain its shape and prevent the need for transplantation. The cost of one treatment using this system is $2,500 to $3,500. A small prospective study including 7 patients with keratoconus was started on a trial of oral riboflavin and 15 minutes of natural sunlight exposure daily. These patients reported no adverse effects and preliminary results showed corneal stabilization and/or corneal flattening in all 7 patients It is hypothesized that dietary riboflavin and natural sunlight is as effective in corneal crosslinking as the currently FDA approved Avedro therapy. If the clinical study confirms the investigators' early observations of the benefits of this approach, coupled with animal studies that document corneal cross-linking, the investigators will have data to pursue funding for larger clinical and animal studies. This has the potential to save millions of dollars in health care costs and ease the burden of treatment in patients who require therapy to induce corneal cross-linking to stabilize the cornea's shape.
Detailed Description
Corneal ectasia as a complication from refractive (LASIK) surgery as well as keratoconus is a slowly progressive condition that results in high patient morbidity. Treatment options aim to stabilize the shape of the cornea using rigid contact lenses, surgical insertion of stiff plastic intrastromal rings, corneal cross linking, and ultimately corneal transplant in severe patients. The recently FDA approved "Dresden Protocol" involves painful cornea scraping followed by application of concentrated Riboflavin, followed by immediate collagen cross linking with UV light exposure which results in shortening and thickening of the collagen fibrils, and therefore a stronger, stiffer cornea. Avedro has demonstrated an average cornea flattening (K max reduction) of 1.4 diopters and 1.7diopters in two different studies. The current cost of Avedro therapy is between $2500 -$3500 per treatment. This is considered experimental at this time and therefore is not covered by any insurance.To spare the patient the severe pain involved in the current procedure, and to avoid the high cost (Avedro is not covered by any medical insurance), the investigator started 7 patients with keratoconus from 2011-2015 in his private practice in Seattle on a trial of oral riboflavin (100 mg or 400 mg daily) and 15 minutes of sunlight exposure daily. No adverse effects have ever been reported with high-dose dietary riboflavin supplements. The results of this preliminary trial are remarkable. During follow-up from 6 months to 5 years, all 7 patients have had corneal stabilization and/or corneal flattening. One patient experienced flattening of the cornea by 1.5 Diopters, comparable to the best results of the Avedro system. A limited animal study is currently underway to document that corneal cross-linking occurs in response to dietary riboflavin and UV exposure from the sun. This clinical study would expand the promising preliminary findings to a larger sample size. This has the potential to save millions of dollars in health care costs and ease the burden of treatment in patients who require therapy to induce corneal cross-linking to stabilize the cornea's shape.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Keratoconus, Cornea Ectasia
Keywords
keratoconus, cornea ectasia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment with riboflavin
Arm Type
Experimental
Arm Description
Patients will take 400 mg dietary riboflavin per day and go outside without sunglasses for 15 minutes per day to evaluate the effects of riboflavin B2 and natural UV light from sun exposure on cornea cross linking and stabilization of ectatic disease.
Intervention Type
Dietary Supplement
Intervention Name(s)
Dietary riboflavin
Other Intervention Name(s)
Vitamin B2
Intervention Description
Dietary riboflavin is vitamin B2. It has been shown to be safe in children in the treatment of migraines at doses of 400 mg per day. There are no known documented side effects
Primary Outcome Measure Information:
Title
Degree of corneal steepening
Description
Keratometry measures the degree of astigmatism of the cornea to monitor the degree of cornea steepening
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Best corrected visual acuity
Description
Measures the best vision the patient is able to see at that time
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: patients identified as having keratoconus or post refractive cornea ectasia with astigmatism of 1.5 Diopters or greater. Exclusion Criteria: Known sensitivity to riboflavin, sunlight. patients on medications with side effects of increased sunlight sensitivity should discuss participation with their prescribing provider prior to participation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
John S Jarstad, MD
Phone
813-821-8022
Email
jarstadj@usf.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Van D Nguyen, MD
Phone
(573) 884-2876
Email
nguyenvd@health.missouri.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John S Jarstad, MD
Organizational Affiliation
University of South Florida - Department of Ophthalmology
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of South Florida Department of Ophthalmology
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John S Jarstad, MD
Phone
813-821-8022
First Name & Middle Initial & Last Name & Degree
John S Jarstad, MD
Phone
2539739116
Email
jarstadj@usf.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Dietary Riboflavin (Vitamin B-2) and Cornea Cross-Linking

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