UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000019591
Receipt number R000022531
Scientific Title The effect of orthokeratology on myopia progression
Date of disclosure of the study information 2015/11/01
Last modified on 2022/11/06 13:24:38

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Basic information

Public title

The effect of orthokeratology on myopia progression

Acronym

Myopia control with orthokeratology

Scientific Title

The effect of orthokeratology on myopia progression

Scientific Title:Acronym

Myopia control with orthokeratology

Region

Japan


Condition

Condition

myopia

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To compare the refractive change and axial length elongation between children receiving orthokeratology treatment and those wearing single-vision spectacles

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

efficacy:
refractive error
axial length

Key secondary outcomes

safety:
corneal endothelial cell density


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Device,equipment

Interventions/Control_1

orthokeratology lens
every overnight wearing throughout the follow-up time

Interventions/Control_2

single-vision spectacles
everyday wearing as necessary throughout follow-up time

Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

6 years-old <=

Age-upper limit

15 years-old >=

Gender

Male and Female

Key inclusion criteria

1) spherical equivalent error: from -4.5D to -1.0D in both eyes
2) astigmatism: <=1.5D in both eyes
3) anisometropia: <=1.5D
4) best-corrected visual acuity: >=0.00 logMAR units in both eyes

Key exclusion criteria

1) ocular diseases except refractive error
2) history of orthokeratology or use of medications

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Shigeru
Middle name
Last name Kinoshita

Organization

Kyoto Prefectural University of Medicine

Division name

Ophthalmology

Zip code

602-8566

Address

465 Kajii-cho Kamigyo-ku Kyoto Japan

TEL

+81-75-251-5578

Email

shigeruk@koto.kpu-m.ac.jp


Public contact

Name of contact person

1st name Yo
Middle name
Last name Nakamura

Organization

Kyoto Prefectural University of Medicine

Division name

Ophthalmology

Zip code

602-8566

Address

465 Kajii-cho Kamigyo-ku Kyoto Japan

TEL

+81-75-251-5578

Homepage URL


Email

yonakamura0108@gmail.com


Sponsor or person

Institute

Kyoto Prefectural University of Medicine

Institute

Department

Personal name



Funding Source

Organization

Kyoto Prefectural University of Medicine

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Institutional Review Board of Kyoto Prefectural University of Medicine

Address

465 Kajii-cho Kamigyo-ku Kyoto Japan

Tel

+81-75-251-5111

Email

rinri@koto.kpu-m.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2015 Year 11 Month 01 Day


Related information

URL releasing protocol

unpublished

Publication of results

Partially published


Result

URL related to results and publications

unpublished

Number of participants that the trial has enrolled

90

Results

In orthokeratology group, myopia progression was suppressed compared in single vision spectacles group.

Results date posted

2021 Year 05 Month 07 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

From 6 to 12 years old children

Participant flow

Subjects wore orthokeratology lens or single vision spectacles for 2 years. Last examination was performed after lens discontinuation peried in the orthokeratology group.

Adverse events

No adverse events

Outcome measures

refractive error change
change of axial length

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2012 Year 05 Month 08 Day

Date of IRB

2012 Year 05 Month 08 Day

Anticipated trial start date

2012 Year 05 Month 08 Day

Last follow-up date

2017 Year 03 Month 30 Day

Date of closure to data entry

2018 Year 03 Month 08 Day

Date trial data considered complete

2019 Year 03 Month 31 Day

Date analysis concluded

2019 Year 09 Month 30 Day


Other

Other related information



Management information

Registered date

2015 Year 11 Month 01 Day

Last modified on

2022 Year 11 Month 06 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022531


Research Plan
Registered date File name
2018/11/05 計画書.doc

Research case data specifications
Registered date File name

Research case data
Registered date File name