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Evaluation of Progression of Myopia in Children Treated With Vitamin B2 and Outdoor Sunlight Exposure

Primary Purpose

Axial Myopia, Refractive Errors

Status
Unknown status
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Oral Riboflavin
Sponsored by
University of Missouri-Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Axial Myopia focused on measuring Myopia, Axial Myopia, Children, Refractive Error, Riboflavin, Vitamin B2

Eligibility Criteria

6 Years - 12 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy children ages 6-12 years old with myopia more than 0.50 D and astigmatism no more than 1.5 D.
  • Caretakers who choose to enroll their child in the study must agree to participate in the study on their own will after knowledge of potential alternatives (spectacle correction, orthokeratology, atropine eye drops, etc.) are explained to the patient's caretaker.

Exclusion Criteria:

  • Known allergy to riboflavin
  • Birth history of premature birth
  • Developmental delay or other neurological or mental conditions
  • Major systemic health problems
  • Significant anisometropia more than 1.5 Diopters
  • Any other eye condition which may complicate interpretation of data including: congenital glaucoma, congenital cataract, ectatic corneal condition, amblyopia or strabismus.

Sites / Locations

  • Eye Institute EastRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

200 mg Riboflavin (oral)

400 mg Riboflavin (oral)

0 mg Riboflavin (oral)

Arm Description

These patients (approximately 1/3rd of all patients enrolled in the study) will be given 200 mg oral riboflavin each day for 6 months and be encouraged to play outside for 30 minutes a day every day.

These patients (approximately 1/3rd of all patients enrolled in the study) will be given 400 mg oral riboflavin each day for 6 months and be encouraged to play outside for 30 minutes a day every day.

These patients (approximately 1/3rd of all patients enrolled in the study) will be given 0 mg oral riboflavin (placebo) each day for 6 months and be encouraged to play outside for 30 minutes a day every day.

Outcomes

Primary Outcome Measures

Change in cycloplegic refraction
We will measure the average change in cycloplegic refraction over 3 years in each treatment/study group.

Secondary Outcome Measures

Change in axial length
Change in axial length over 3 years in each treatment/study group.
Change in keratometry values
Change in keratometry values over 3 years in each study group.
Change in uncorrected best visual acuity
Change in uncorrected best visual acuity over 3 years in each study group.

Full Information

First Posted
May 28, 2018
Last Updated
April 16, 2021
Sponsor
University of Missouri-Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT03552016
Brief Title
Evaluation of Progression of Myopia in Children Treated With Vitamin B2 and Outdoor Sunlight Exposure
Official Title
Evaluation of Progression of Myopia in Children Treated With Vitamin B2 and Outdoor Sunlight Exposure
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
October 10, 2018 (Actual)
Primary Completion Date
October 10, 2021 (Anticipated)
Study Completion Date
October 10, 2023 (Anticipated)

3. Sponsor/Collaborators

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

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators plan on using riboflavin (a Vitamin that can easily be taken orally each day) and having the children involved in the study play outside (where there is UV light created by the sun) in order to prevent the eye from becoming progressively more near-sighted.
Detailed Description
Myopia is equivalent to the colloquial term known as near-sightedness. This, in short, means that the image of one's environment is projected in front of the retina (rather than directly on the retina, which is ideal). Of course, glasses can be used to correct the image disparity that is created by being near-sighted (that is why a lot of people need glasses for blurry vision). However, glasses and spectacles and contacts do not correct the underlying problem. Most near-sightedness is due to the eye being "too long" and therefore the image projects in front of the retina. Ideally, if we could prevent the eye from becoming abnormally "long", then we could prevent the progression of near-sightedness. Indeed, a child may only be slightly near-sighted early in life, but as he/she continues to perform activities within an arms length of their environment, they can become progressively near-sighted. Besides spectacle correction, people have tried topical atropine drops (medicated eye drops) and rigid contact lenses (orthokeratology) to attempt to correct near-sightedness. Atropine drops take a lot of cooperation from parent and child. Orthokeratology also requires a lot of cooperation, but also, does not permanently stall myopic progression. The investigators suggest a different means of potentially preventing near-sightedness from getting worse (and thus prevent the eye from getting "too long"). The investigators plan on using riboflavin (a Vitamin that can easily be taken orally each day) and having the children involved in the study play outside (where there is UV light created by the sun) in order to prevent the eye from becoming progressively more near-sighted.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Axial Myopia, Refractive Errors
Keywords
Myopia, Axial Myopia, Children, Refractive Error, Riboflavin, Vitamin B2

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
This is a 1:1:1 double-blinded randomized study for children ages 6-12 year old with axial myopia who will be treated with one of three different doses of oral riboflavin. Expected number of participants is 100.
Masking
ParticipantCare ProviderInvestigator
Masking Description
The researchers involved, the project investigator, and the patients will be blinded from knowing which patient will get which treatment by assigning a number to each patient and having that patient take that number to the pharmacy where they will pick up their riboflavin. The dosage of riboflavin given to the patient will be chosen by the "number" that the patient gives to the pharmacy. There will be no labels revealing the dose of riboflavin that the patient receives. There will be placebo dose which contains a small dose of riboflavin that has been shown to not reach therapeutic levels.
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
200 mg Riboflavin (oral)
Arm Type
Experimental
Arm Description
These patients (approximately 1/3rd of all patients enrolled in the study) will be given 200 mg oral riboflavin each day for 6 months and be encouraged to play outside for 30 minutes a day every day.
Arm Title
400 mg Riboflavin (oral)
Arm Type
Experimental
Arm Description
These patients (approximately 1/3rd of all patients enrolled in the study) will be given 400 mg oral riboflavin each day for 6 months and be encouraged to play outside for 30 minutes a day every day.
Arm Title
0 mg Riboflavin (oral)
Arm Type
Placebo Comparator
Arm Description
These patients (approximately 1/3rd of all patients enrolled in the study) will be given 0 mg oral riboflavin (placebo) each day for 6 months and be encouraged to play outside for 30 minutes a day every day.
Intervention Type
Drug
Intervention Name(s)
Oral Riboflavin
Other Intervention Name(s)
Vitamin B2
Intervention Description
The intervention doses will be 200 mg oral riboflavin and 400 mg oral riboflavin doses; the placebo dose will be 0 mg of oral riboflavin
Primary Outcome Measure Information:
Title
Change in cycloplegic refraction
Description
We will measure the average change in cycloplegic refraction over 3 years in each treatment/study group.
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Change in axial length
Description
Change in axial length over 3 years in each treatment/study group.
Time Frame
3 years
Title
Change in keratometry values
Description
Change in keratometry values over 3 years in each study group.
Time Frame
3 years
Title
Change in uncorrected best visual acuity
Description
Change in uncorrected best visual acuity over 3 years in each study group.
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy children ages 6-12 years old with myopia more than 0.50 D and astigmatism no more than 1.5 D. Caretakers who choose to enroll their child in the study must agree to participate in the study on their own will after knowledge of potential alternatives (spectacle correction, orthokeratology, atropine eye drops, etc.) are explained to the patient's caretaker. Exclusion Criteria: Known allergy to riboflavin Birth history of premature birth Developmental delay or other neurological or mental conditions Major systemic health problems Significant anisometropia more than 1.5 Diopters Any other eye condition which may complicate interpretation of data including: congenital glaucoma, congenital cataract, ectatic corneal condition, amblyopia or strabismus.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mohannad Al-Samarraie, MD
Phone
573-882-1506
Email
alsamarraiem@health.missouri.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Ryan N Mercer, MD
Phone
803-740-9673
Email
mercerr@health.missouri.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohannad Al-Samarraie, MD
Organizational Affiliation
University of Missouri-Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Eye Institute East
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65201
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mohannad Al-Samarraie, MD
Phone
573-882-7389
Email
alsamarraiem@health.missouri.edu
Phone
573-882-8920

12. IPD Sharing Statement

Plan to Share IPD
No

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Evaluation of Progression of Myopia in Children Treated With Vitamin B2 and Outdoor Sunlight Exposure

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