UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000047316
Receipt number R000053901
Scientific Title Examination of retinal scanning laser eyewear for patients with corneal irregular astigmatism
Date of disclosure of the study information 2022/03/29
Last modified on 2022/03/29 19:23:13

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Basic information

Public title

Examination of retinal scanning laser eyewear for patients with corneal irregular astigmatism

Acronym

Retinal scanning laser eyewear for patients with corneal irregular astigmatism

Scientific Title

Examination of retinal scanning laser eyewear for patients with corneal irregular astigmatism

Scientific Title:Acronym

Retinal scanning laser eyewear for patients with corneal irregular astigmatism

Region

Japan


Condition

Condition

corneal irregular astigmatism

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to measure visual acuity of patients with corneal irregular astigmatism.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Sex, age, visual acuity, refraction, slit-lamp microscopy, corneal topography

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients with corneal irregular astigmatism

Key exclusion criteria

Patients with optic nerve disorder or retinopathy

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Yuichi
Middle name
Last name Hori

Organization

Toho University Omori medical center

Division name

Ophthalmology

Zip code

143-8541

Address

6-11-1, Omorinishi, Ota-ku, Tokyo

TEL

0337624151

Email

yhori@med.toho-u.ac.jp


Public contact

Name of contact person

1st name Sayaka
Middle name
Last name Sumazaki

Organization

Toho University, Omori medical center

Division name

Ophthalmology

Zip code

143-8541

Address

6-11-1, Omorinishi, Ota-ku, Tokyo

TEL

0337624151

Homepage URL


Email

sayaka.sumazaki@med.toho-u.ac.jp


Sponsor or person

Institute

Toho University, Omori medical center

Institute

Department

Personal name



Funding Source

Organization

Self funding

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

Ethics Committee of Toho University Omori Medical Center

Address

6-11-1, Omorinishi, Ota-ku, Tokyo

Tel

0337624151

Email

omori.rinri@ext.toho-u.ac.jp


Secondary IDs

Secondary IDs

YES

Study ID_1

M21192

Org. issuing International ID_1

Ethics Committee of Toho University Omori Medical Center

Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2022 Year 03 Month 29 Day


Related information

URL releasing protocol


Publication of results

Unpublished


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

2022 Year 02 Month 22 Day

Date of IRB

2022 Year 02 Month 22 Day

Anticipated trial start date

2022 Year 02 Month 22 Day

Last follow-up date

2024 Year 08 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

observational study


Management information

Registered date

2022 Year 03 Month 29 Day

Last modified on

2022 Year 03 Month 29 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000053901