UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000052524
Receipt number R000047834
Scientific Title Evaluation of mono vision using intraocular lens in cases with laterality in axial length
Date of disclosure of the study information 2023/10/18
Last modified on 2023/10/17 19:10:39

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Basic information

Public title

Evaluation of mono vision using intraocular lens in cases with laterality in axial length

Acronym

Mono vision with intraocular lens in cases with laterality in axial length

Scientific Title

Evaluation of mono vision using intraocular lens in cases with laterality in axial length

Scientific Title:Acronym

Mono vision with intraocular lens in cases with laterality in axial length

Region

Japan


Condition

Condition

cataract

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate mono vision using intraocular lens for cases with laterality in axial length

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

refractive error, distance visual acuity, near visual acuity, multi-distance visual acuity, contrast sensitivity, aniseikonia test, stereopsis test in one month post-operative period

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

We implanted intraocular lens for distance targeted intraocular lens in eyes with longer axial length and near targeted one in eyes with shorter axial length in patient underwent bilateral cataract surgery.

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

Patient having bilateral cataract surgery with longer than 0.5mm laterality in axial length

Key exclusion criteria

Patient with laterality in axial length shorter than 0.5mm

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Masayuki
Middle name
Last name Ouchi

Organization

Masayuki Ouchi Eye Clinic

Division name

Ophthalmology

Zip code

6018449

Address

9 Nishikujo Ohkuni-cho Minami-ku, Kyoto 601-8449, Japan

TEL

075-662-5660

Email

mouchi@skyblue.ocn.ne.jp


Public contact

Name of contact person

1st name Masayuki
Middle name
Last name Ouchi

Organization

Masayuki Ouchi Eye Clinic

Division name

Ophthalmology

Zip code

6018449

Address

9 Nishikujo Ohkuni-cho Minami-ku, Kyoto 601-8449, Japan

TEL

075-662-5660

Homepage URL


Email

mouchi@skyblue.ocn.ne.jp


Sponsor or person

Institute

Masayuki Ouchi Eye Clinic

Institute

Department

Personal name



Funding Source

Organization

none

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 Masayuki Ouchi Eye Clinic

Address

9 Nishikujo Ohkuni-cho Minami-ku, Kyoto 601-8449, Japan

Tel

075-662-5660

Email

mouchi@skyblue.ocn.ne.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 10 Month 18 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

42

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

No longer recruiting

Date of protocol fixation

2020 Year 12 Month 01 Day

Date of IRB

2023 Year 01 Month 14 Day

Anticipated trial start date

2020 Year 12 Month 02 Day

Last follow-up date

2023 Year 10 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2023 Year 10 Month 17 Day

Last modified on

2023 Year 10 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000047834


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name