Efficacy and Safety of cleadewGP for Rigid Contact Lenses

Sponsor
The Hong Kong Polytechnic University (Other)
Overall Status
Completed
CT.gov ID
NCT03193255
Collaborator
OPHTECS Corporation (Other)
80
1
4
25.6
3.1

Study Details

Study Description

Brief Summary

Multipurpose solutions (MPS) are the most commonly prescribed regimen to clean, disinfect and rinse rigid lenses. The preservatives used in MPS may cause hypersensitivity and the presence of quaternary ammonium compounds (QAC) may increase development of antiseptic resistance mediated by QAC resistance genes, thus lowering the efficacy of disinfection. Povidone-iodine (PVI) has been safely used as a disinfectant for ophthalmic operations and eye drops. The cleadew GP (Ophtecs, Japan) tested in the current study is a PVI based rigid lens disinfecting solutions which does not employ QAC. If its efficacy and safety can be confirmed in this study, it will be a good alternative rigid lens care regimen for children.

Condition or Disease Intervention/Treatment Phase
  • Device: OPHTECS cleadew GP
N/A

Detailed Description

Multipurpose solutions (MPS) are the most commonly prescribed regimen to clean, disinfect and rinse rigid lenses. These solutions usually contain quaternary ammonium compounds (QAC) which have been shown to be selective for carriage of organisms harbouring QAC genes in orthokeratology (ortho-k) lens wear and it raises concerns about safety with the increasing popularity of orthokeratology (ortho-k) for myopia control in children. Hydrogen peroxide system is a good alternative but this option is limited in rigid lens market. The only brand available in Hong Kong labelled as safe for rigid contact lenses has limited disinfecting power. cleadewGP (Ophtecs, Japan) is a new disinfecting solution for rigid contact lenses which does not employ QAC and instead is povidone iodine (PVI) based. PVI has been safely used as a disinfectant for ophthalmic operations and is commonly used in eye drops. PVI-based soft and rigid lens solutions have been reported to be as effective against Pseudomonas aeruginosa as other MPS and hydrogen peroxide-based solutions. However, other efficacy against other organisms need to be demonstrated to allow this solution to meet FDA requirements. The PVI-based soft lens solution was also reported to be effective against Acanthamoeba. cleadewGP is relatively new in the market and not much work has been done on the efficacy and safety of this solution. If confirmed to be effective and safe, cleadewGP may be a better alternative to ortho-k lens wearers who need to use disinfecting solutions at least for a few years while under ortho-k treatment. In the absence of QAC, there will be no concern of selection of carriage of organisms harbouring QAC genes in ortho-k lens wearers using this disinfecting solution over time.

The current study aims at investigating the effectiveness and safety of the cleadewGP for cleaning (lipid and protein removal) and disinfecting of ortho-k lenses by comparing the outcomes collected from subjects randomly assigned to one of the following study groups.

Group 1: cleadewGP without lens rubbing Group 2: cleadewGP with lens rubbing Group 3:

cleadewGP with separate daily cleaner Group 4: cleadewGP with separate daily cleaner and weekly protein removal agent

Four study visits will be involved in this 6 months study: baseline, 1-month, 3-month, and 6-month after lens wear. Complimentary solutions will be provided during the study period. Solutions and accessories will be replaced at monthly interval. Effectiveness for cleaning and disinfection and safety of lens wear will be determined by comparing the changes in ocular microbiome before and after lens wear, contamination levels of lenses and accessories, biomicroscopic examination of lenses and eyes, and subjective rating of lens comfort among the four groups of subjects.

Study Design

Study Type:
Interventional
Actual Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Efficacy and Safety of Povidone Iodine-based Disinfecting Solution (cleadewGP) for Rigid Contact Lenses
Actual Study Start Date :
Jun 14, 2017
Actual Primary Completion Date :
Aug 1, 2019
Actual Study Completion Date :
Aug 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: No daily lens rubbing

Daily lens disinfection with OPHTECS cleadew GP without lens rubbing

Device: OPHTECS cleadew GP
Povidone-iodine based disinfecting solutions for rigid contact lenses

Active Comparator: Daily rubbing

Daily lens disinfection with OPHTECS cleadew GP after lens rubbing with cleadew GP

Device: OPHTECS cleadew GP
Povidone-iodine based disinfecting solutions for rigid contact lenses

Active Comparator: Daily rubbing with separate cleaner

Daily lens disinfection with OPHTECS cleadew GP after lens rubbing with a daily lipid cleaner

Device: OPHTECS cleadew GP
Povidone-iodine based disinfecting solutions for rigid contact lenses

Active Comparator: Daily rubbing and weekly protein removal

Daily lens disinfection with OPHTECS cleadew GP after daily lipid cleaner followed by weekly protein removal treatment

Device: OPHTECS cleadew GP
Povidone-iodine based disinfecting solutions for rigid contact lenses

Outcome Measures

Primary Outcome Measures

  1. Change in subjective symptoms before and 6 months after lens wear [6 months]

    Questionnaire of ocular comfort will be administered to rate symptoms of discomfort, itching, tearing, dryness and redness

  2. Change in corneal staining and injection before and 6 months after ortho-k lens wear [6 months]

    Grading of corneal staining, limbal injection and conjunctival injection under slitlamp biomicroscopy before and after ortho-k lens wear

Secondary Outcome Measures

  1. Change in levels of ocular microbiome before and 6 months after ortho-k lens wear [6 months]

    Sample from the lower conjunctiva will be gently taken with cotton swab pre-wet with normal saline before and ortho-k lens wear

  2. Levels of contamination of lens cases [6 months]

    Sample will be collected from the left compartment of the lens case to determine the presence of microorganisms. The right compartment of the lens case will be tested for the presence and amount of biofilm

  3. Levels of contamination of lenses [6 months]

    Samples will be collected from the left lens surface to test for the presence of microorganisms

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 10 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • cycloplegic objective sphere between -1.00D to -4.00D

  • cycloplegic objective astigmatism ≤ 2.00D

  • anisometropia < 1.00D

  • best-corrected logMAR visual acuity 0.10 or better in both eyes

  • symmetrical corneal topography with toricity ≤ 2.00D

  • normal ocular health

Exclusion Criteria:
  • contraindication to ortho-k wear

  • prior history of myopia control treatment

  • prior history of rigid contact lens wear

  • strabismus or amblyopia

  • systemic or ocular conditions which might affect refractive development

  • poor response or poor compliance to lens wear including poor lens handling, poor vision, and/ocular response after lens modifications

Contacts and Locations

Locations

Site City State Country Postal Code
1 School of Optometry, The Hong Kong Polytechnic University Kowloon Hong Kong

Sponsors and Collaborators

  • The Hong Kong Polytechnic University
  • OPHTECS Corporation

Investigators

  • Principal Investigator: Pauline Cho, PhD, The Hong Kong Polytechnic University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Pauline Cho, Professor, The Hong Kong Polytechnic University
ClinicalTrials.gov Identifier:
NCT03193255
Other Study ID Numbers:
  • HSEARS20170430002
First Posted:
Jun 20, 2017
Last Update Posted:
Feb 16, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Feb 16, 2021