UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000053944
Receipt number R000061568
Scientific Title Effect of postoperative corneal edema on visual acuity in posterior chamber intraocular collamer lens
Date of disclosure of the study information 2024/03/23
Last modified on 2024/03/22 16:40:47

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Basic information

Public title

Effect of postoperative corneal edema on visual acuity in posterior chamber intraocular collamer lens

Acronym

Effect of postoperative corneal edema on visual acuity in posterior chamber intraocular collamer lens

Scientific Title

Effect of postoperative corneal edema on visual acuity in posterior chamber intraocular collamer lens

Scientific Title:Acronym

Effect of postoperative corneal edema on visual acuity in posterior chamber intraocular collamer lens

Region

Japan


Condition

Condition

Myopic astigmatism

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the effect of postoperative corneal edema on visual acuity in ICL

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Central corneal thickness

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

50 years-old >

Gender

Male and Female

Key inclusion criteria

(1) Cases in which ICL surgery was performed at Chukyo Eye Clinic during the period from December 1, 2018 ~ October 31, 2023
(2) Cases in which the surgery was completed according to the conventional procedure

Key exclusion criteria

(1) Patients with a history of eye diseases other than refractive error and dry eye (keratoconus, ocular inflammatory disease, ocular infection, cataract, glaucoma, retinal disease, etc.) or other ophthalmic surgery
(2) Cases judged by the principal investigator to be inappropriate
(3) Cases in which unforeseen circumstances occurred during surgery and deviated from the conventional ICL surgical procedure
(4) Reoperation cases

Target sample size

350


Research contact person

Name of lead principal investigator

1st name satoshi
Middle name
Last name gotoda

Organization

Chukyo eye clinic

Division name

Ophthalmology

Zip code

4560032

Address

12-22 Sanbonmatsu-cho, Atsuta-ku, Nagoya City, Aichi Prefecture

TEL

0528831543

Email

sgotoda@chukyo-eyeclinic.jp


Public contact

Name of contact person

1st name satoshi
Middle name
Last name gotoda

Organization

Chukyo Eye Clinic

Division name

Ophthalmology

Zip code

456-0032

Address

12-22 Sanbonmatsu-cho, Atsuta-ku, Nagoya City, Aichi Prefecture

TEL

0528831543

Homepage URL


Email

sgotoda@chukyo-eyeclinic.jp


Sponsor or person

Institute

Chukyo eye clinic

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

Chukyo Eye Clinic Ethics Review Committee

Address

12-22 Sanbonmatsu-cho, Atsuta-ku, Nagoya City, Aichi Prefecture

Tel

0528831543

Email

snimi@chukyomedical.co.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

2024 Year 03 Month 23 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

98

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

2023 Year 12 Month 01 Day

Date of IRB

2023 Year 12 Month 22 Day

Anticipated trial start date

2023 Year 12 Month 24 Day

Last follow-up date

2026 Year 12 Month 24 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

not particular


Management information

Registered date

2024 Year 03 Month 22 Day

Last modified on

2024 Year 03 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000061568