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Variation of Orthokeratology Lens Treatment Zone (VOLTZ) Study

Primary Purpose

Myopia

Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Modified ortho-k lenses
Ortho-k lenses
Sponsored by
The Hong Kong Polytechnic University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myopia focused on measuring Myopia control, Orthokeratology, Children, Treatment zone

Eligibility Criteria

6 Years - 11 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Manifest myopia between 1.00-4.00D in both eyes at screening visit
  • Manifest astigmatism ≤2.50D; with-the-rule astigmatism (axes 180 ± 30)

    • 2.50D; astigmatism with other axes ≤0.50D in both eyes at screening visit
  • <1.00D difference in manifest spherical equivalent (SE) between the two eyes at screening visit
  • Baseline cycloplegic objective refraction between 1.00-4.00D in sphere; astigmatism ≤2.50D; <1.00D difference in manifest SE between the two eyes
  • Best-corrected logMAR visual acuity 0.10 or better in both eyes Symmetrical corneal topography with corneal toricity <2.00D in either eye
  • Normal ocular health other than myopia
  • Agree to be randomized and to attend the scheduled visits and aftercare

Exclusion Criteria:

  • Contraindications to atropine: known allergies or cardiovascular disease, epilepsy
  • Contraindications to contact lens wear and ortho-k: corneal scar, history of ocular inflammation/infection, limbus-to-limbus corneal cylinder and dislocated corneal apex
  • Strabismus or amblyopia
  • History of myopia control treatment (e.g. soft contact lenses, progressive add spectacles, atropine eye drops)
  • Rigid contact lens (including ortho-k) wear experience
  • Systemic condition which might affect refractive development (for example, Down syndrome, Marfan's syndrome)
  • Ocular conditions which might affect refractive error (for example, cataract, ptosis)
  • Poor response to lens wear including poor lens handling, poor vision and/ocular response after lens modifications
  • Poor compliance with schedule visits

Sites / Locations

  • School of Optometry, The Hong Kong Polytechnic University
  • School of Optometry

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Modified ortho-k lenses

Ortho-k lenses

Arm Description

Participants wearing ortho-k lens with a modified BOZD of 5mm

Participants wearing ortho-k lens with a standardized BOZD of 6mm

Outcomes

Primary Outcome Measures

Change in axial length before and after two years of lens wear
To determine the change in axial length measured at baseline and two years after lens wear using IOLMaster

Secondary Outcome Measures

Treatment zone characteristics
Corneal topography will be determined by Medmont topographer and the treatment zone characteristics will be determined from the subtractive maps
Pupil sizes
Photopic and mesotopic pupil sizes
Choroidal thickness
Choroidal thickness measurement will be determined by both LenStar and posterior OCT

Full Information

First Posted
June 14, 2017
Last Updated
July 18, 2022
Sponsor
The Hong Kong Polytechnic University
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1. Study Identification

Unique Protocol Identification Number
NCT03191942
Brief Title
Variation of Orthokeratology Lens Treatment Zone (VOLTZ) Study
Official Title
Variation of Orthokeratology Lens Treatment Zone (VOLTZ) Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
June 20, 2017 (Actual)
Primary Completion Date
March 21, 2021 (Actual)
Study Completion Date
July 27, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Hong Kong Polytechnic University

4. Oversight

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

5. Study Description

Brief Summary
This project aims to study the effects of treatment characteristics on myopia control in orthokeratology by investigating the effects of modified treatment zone by reducing the lens back optic zone diameter on the effect of myopia control. The project will be a two-year randomized, double-masked (examiner - mask axial length only) study conducted at The Hong Kong Polytechnic University recruiting sixty Chinese subjects aged between 6-11. Subjects will be randomly assigned to two ortho-k groups. The Control group will wear KATT BeFree lens with a BOZD of 6mm while the Test group will wear KATT MC lens with a modified BOZD of 5mm.
Detailed Description
Orthokeratology (Ortho-k) treatment reduces the degree of myopia of the eye by flattening the central cornea. This central flattened zone is referred to as the treatment zone (TZ). Munnerlyn's formula describes the negative correlation between refractive correction and treatment zone size given a maximum ablation depth limited by the patient's corneal thickness in refractive surgery. This implies smaller TZ for higher myopic reduction and, indeed, a study found marginally smaller TZ of 0.3mm in higher myopic group. In ortho-k, it has been speculated that TZ may be associated with the effect of the treatment. The TZ is defined as the central flattened area enclosed by points with zero power/curvature changes comparing to pre-treatment condition on various topography maps. Previous studies determine the TZ characteristics based on different types of topographical subtractive maps including tangential, axial and refractive maps. A study compared TZ parameters derived from the three different maps. The study defined the TZ as the area enclosed by zero power change in different subtractive maps; 12 such points equally spaced 30 degree apart to construct a best-fit ellipse. Geometrical center of this ellipse was used to determine the TZ decentration and TZ diameter along vertical and horizontal axes. The study found significantly less TZ decentration and diameter in tangential map comparing to axial and refractive maps and no significant difference between the latter two. Based on these findings, the investigators suggested that either refractive or axial map would be of high validity and accuracy in determining TZ characteristics. The current study would investigate the effect of TZ on myopic control in ortho-k. TZ, defined as the area enclosed by zero power change in subjective maps will be employed. The tangential and refractive subtractive maps will be used to determine the TZ. Characteristics of the TZ, including diameter, slope, depth, volume, would be analyzed based on topographical subtractive maps and the effect of each of these characteristics on myopia control will be evaluated. The role of pupil size during normal viewing condition (distance and near) will also be investigated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myopia
Keywords
Myopia control, Orthokeratology, Children, Treatment zone

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Modified ortho-k lenses
Arm Type
Experimental
Arm Description
Participants wearing ortho-k lens with a modified BOZD of 5mm
Arm Title
Ortho-k lenses
Arm Type
Active Comparator
Arm Description
Participants wearing ortho-k lens with a standardized BOZD of 6mm
Intervention Type
Device
Intervention Name(s)
Modified ortho-k lenses
Intervention Description
KETT MC lens
Intervention Type
Device
Intervention Name(s)
Ortho-k lenses
Intervention Description
KATT BeFree lens
Primary Outcome Measure Information:
Title
Change in axial length before and after two years of lens wear
Description
To determine the change in axial length measured at baseline and two years after lens wear using IOLMaster
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Treatment zone characteristics
Description
Corneal topography will be determined by Medmont topographer and the treatment zone characteristics will be determined from the subtractive maps
Time Frame
2 years
Title
Pupil sizes
Description
Photopic and mesotopic pupil sizes
Time Frame
2 years
Title
Choroidal thickness
Description
Choroidal thickness measurement will be determined by both LenStar and posterior OCT
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Manifest myopia between 1.00-4.00D in both eyes at screening visit Manifest astigmatism ≤2.50D; with-the-rule astigmatism (axes 180 ± 30) 2.50D; astigmatism with other axes ≤0.50D in both eyes at screening visit <1.00D difference in manifest spherical equivalent (SE) between the two eyes at screening visit Baseline cycloplegic objective refraction between 1.00-4.00D in sphere; astigmatism ≤2.50D; <1.00D difference in manifest SE between the two eyes Best-corrected logMAR visual acuity 0.10 or better in both eyes Symmetrical corneal topography with corneal toricity <2.00D in either eye Normal ocular health other than myopia Agree to be randomized and to attend the scheduled visits and aftercare Exclusion Criteria: Contraindications to atropine: known allergies or cardiovascular disease, epilepsy Contraindications to contact lens wear and ortho-k: corneal scar, history of ocular inflammation/infection, limbus-to-limbus corneal cylinder and dislocated corneal apex Strabismus or amblyopia History of myopia control treatment (e.g. soft contact lenses, progressive add spectacles, atropine eye drops) Rigid contact lens (including ortho-k) wear experience Systemic condition which might affect refractive development (for example, Down syndrome, Marfan's syndrome) Ocular conditions which might affect refractive error (for example, cataract, ptosis) Poor response to lens wear including poor lens handling, poor vision and/ocular response after lens modifications Poor compliance with schedule visits
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pauline Cho, phd
Organizational Affiliation
The Hong Kong Polytechnic University
Official's Role
Principal Investigator
Facility Information:
Facility Name
School of Optometry, The Hong Kong Polytechnic University
City
Kowloon
Country
Hong Kong
Facility Name
School of Optometry
City
Kowloon
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
15201715
Citation
Owens H, Garner LF, Craig JP, Gamble G. Posterior corneal changes with orthokeratology. Optom Vis Sci. 2004 Jun;81(6):421-6. doi: 10.1097/01.opx.0000135097.99877.5d.
Results Reference
background
PubMed Identifier
17956362
Citation
Lu F, Simpson T, Sorbara L, Fonn D. The relationship between the treatment zone diameter and visual, optical and subjective performance in Corneal Refractive Therapy lens wearers. Ophthalmic Physiol Opt. 2007 Nov;27(6):568-78. doi: 10.1111/j.1475-1313.2007.00520.x.
Results Reference
background
PubMed Identifier
19663928
Citation
Gifford P, Swarbrick HA. The effect of treatment zone diameter in hyperopic orthokeratology. Ophthalmic Physiol Opt. 2009 Nov;29(6):584-92. doi: 10.1111/j.1475-1313.2009.00672.x. Epub 2009 Aug 3.
Results Reference
background
PubMed Identifier
14688542
Citation
Tahhan N, Du Toit R, Papas E, Chung H, La Hood D, Holden AB. Comparison of reverse-geometry lens designs for overnight orthokeratology. Optom Vis Sci. 2003 Dec;80(12):796-804. doi: 10.1097/00006324-200312000-00009.
Results Reference
background
PubMed Identifier
12637831
Citation
Sridharan R, Swarbrick H. Corneal response to short-term orthokeratology lens wear. Optom Vis Sci. 2003 Mar;80(3):200-6. doi: 10.1097/00006324-200303000-00009.
Results Reference
background
PubMed Identifier
3339547
Citation
Munnerlyn CR, Koons SJ, Marshall J. Photorefractive keratectomy: a technique for laser refractive surgery. J Cataract Refract Surg. 1988 Jan;14(1):46-52. doi: 10.1016/s0886-3350(88)80063-4.
Results Reference
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Variation of Orthokeratology Lens Treatment Zone (VOLTZ) Study

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