UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000050608
Receipt number R000057644
Scientific Title Investigating the effects of treatment for diseases that cause visual dysfunction on the eye
Date of disclosure of the study information 2023/04/05
Last modified on 2023/05/01 23:30:03

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Basic information

Public title

Investigating the effects of treatment for diseases that cause visual dysfunction on the eye

Acronym

Investigating the effects of treatment for diseases that cause visual dysfunction on the eye

Scientific Title

Investigating the effects of treatment for diseases that cause visual dysfunction on the eye

Scientific Title:Acronym

Investigating the effects of treatment for diseases that cause visual dysfunction on the eye

Region

Japan


Condition

Condition

Investigation of the effects of treatment for diseases that cause visual dysfunction on the eye.

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the effects of drug and surgical treatments for diseases that cause visual dysfunction on the eye on the eye and to identify findings that can be used to make better treatment choices.

Basic objectives2

Others

Basic objectives -Others

To determine the impact of treatment on the eye and changes in findings over time based on visual acuity, visual field and other visual function tests before and after treatment, intraocular pressure, postoperative quality of life, imaging findings, videos during the surgery etc.

Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Finding factors allows estimation of best-corrected visual acuity and visual field before and after treatment for diseases that cause visual dysfunction on the eye based on pretreatment findings and patient characteristics.

Key secondary outcomes

Finding the effects of treatment on the eye and changes in findings over time will be examined based on visual acuity, visual field and other visual function tests before and after treatment, intraocular pressure, postoperative quality of life, imaging findings, etc.


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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients who are scheduled to receive treatment for endophthalmic diseases (lens disease, glaucoma, ocular inflammatory disease, vitreoretinal disease, choroidal disease, etc.) at the Department of Ophthalmology, Nagoya University Hospital between the date of approval for implementation and December 31, 2025. Patients undergoing follow-up observation with a view to future treatment are also eligible.
Gender and age are not required.

Key exclusion criteria

Patients who do not have reliable visual function tests

Target sample size

1000


Research contact person

Name of lead principal investigator

1st name Kenya
Middle name
Last name Yuki

Organization

Nagoya University Graduate School of Medicine

Division name

Department of Ophthalmology

Zip code

4668560

Address

65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, Japan

TEL

+81-52-744-2275

Email

tomitaryo@med.nagoya-u.ac.jp


Public contact

Name of contact person

1st name Ryo
Middle name
Last name Tomita

Organization

Nagoya University Graduate School of Medicine

Division name

Department of Ophthalmology

Zip code

4668560

Address

65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, Japan

TEL

81-52-744-2275

Homepage URL


Email

tomitaryo@med.nagoya-u.ac.jp


Sponsor or person

Institute

Nagoya University

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Nagoya University Hospital

Address

65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, Japan

Tel

+81-52-744-2275

Email

ethics@med.nagoya-u.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

2023 Year 04 Month 05 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

Preinitiation

Date of protocol fixation

2023 Year 02 Month 28 Day

Date of IRB


Anticipated trial start date

2023 Year 04 Month 15 Day

Last follow-up date

2025 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

To find factors in which the best corrected visual acuity and visual field before and after treatment for diseases that cause visual dysfunction on the eye can be inferred from pretreatment findings and patient characteristics.


Management information

Registered date

2023 Year 03 Month 16 Day

Last modified on

2023 Year 05 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000057644


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name