UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000028768
Receipt number R000032904
Scientific Title Suppression of myopia progression by low dose atropine
Date of disclosure of the study information 2017/08/25
Last modified on 2017/08/22 10:11:50

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Basic information

Public title

Suppression of myopia progression by low dose atropine

Acronym

Suppression of myopia progression by low dose atropine

Scientific Title

Suppression of myopia progression by low dose atropine

Scientific Title:Acronym

Suppression of myopia progression by low dose atropine

Region

Japan


Condition

Condition

Childhood Myopia

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Study on suppression effect of childhood myopia progression with low dose atropine(0.01%).

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Myopia progression at 4 year
Cycloplegic subjective refraction
Axial length

Key secondary outcomes

Distance best-corrected visual acuity logMAR
Near visual acuity was assessed using best corrected distance spectacle correction with a reduced logMAR reading chart
Pupil diameter
Accommodation amplitude


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

0.01% atropine
Once a day
4 year
Single vision lenses

Interventions/Control_2

Single vision lenses

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

12 years-old >=

Gender

Male and Female

Key inclusion criteria

Spherical equivalent -1.50D~-4.50D
Astigmatism of less than 1.5D

Key exclusion criteria

A case with ocular disease other than myopia

Target sample size

80


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kyoko Ohno-Matsui

Organization

Tokyo Medical and Dental University

Division name

Ophthalmology&Visual Science

Zip code


Address

1-5-45 Yushima,Bunkyo-ku,Tokyo,Japan113-8519

TEL

03-3813-6111

Email

k.ohno.oph@tmd.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Yuki Nishiyama

Organization

Tokyo Medical and Dental University

Division name

Ophthalmology&Visual Science

Zip code


Address

1-5-45 Yushima,Bunkyo-ku,Tokyo,Japan113-8519

TEL

03-3813-6111

Homepage URL


Email

ynishiyama-tmd@umin.ac.jp


Sponsor or person

Institute

Tokyo Medical and Dental University

Institute

Department

Personal name



Funding Source

Organization

Tokyo Medical and Dental University

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

YES

Study ID_1

M2000-1638

Org. issuing International ID_1

Tokyo Medical and Dental University

Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

東京医科歯科大学医学部附属病院(東京都)


Other administrative information

Date of disclosure of the study information

2017 Year 08 Month 25 Day


Related information

URL releasing protocol


Publication of results

Partially published


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Open public recruiting

Date of protocol fixation

2014 Year 02 Month 12 Day

Date of IRB


Anticipated trial start date

2014 Year 02 Month 12 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 08 Month 22 Day

Last modified on

2017 Year 08 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000032904


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name