UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000041469
Receipt number R000046706
Scientific Title Comparison of 5-year treatment result of laser photocoagulation and intravitreal injection of bevacizumab for retinopathy of prematurity
Date of disclosure of the study information 2020/08/21
Last modified on 2022/03/23 16:41:41

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Basic information

Public title

Comparison of 5-year treatment result of laser photocoagulation and intravitreal injection of bevacizumab for retinopathy of prematurity

Acronym

Treatment result of intravitreal injection of bevacizumab for retinopathy of prematurity

Scientific Title

Comparison of 5-year treatment result of laser photocoagulation and intravitreal injection of bevacizumab for retinopathy of prematurity

Scientific Title:Acronym

Treatment result of intravitreal injection of bevacizumab for retinopathy of prematurity

Region

Japan


Condition

Condition

Retinopathy of prematurity

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to compare the treatment results and safety at the age of 5 between the laser group and the intravitreal injection of bevacizumab group.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Visual acuity at the age of 5

Key secondary outcomes

Equivalent spherical value, ocular complications and mental retardation at the age of 5


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

5 years-old >=

Gender

Male and Female

Key inclusion criteria

Patients who underwent laser photocoagulation or intravitreal injection of bevacizumab for retinopathy of prematurity.

Key exclusion criteria

Patients who did not have at least 5 years of follow-up.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Yoshimi
Middle name
Last name Sugiura

Organization

University of Tsukuba

Division name

Department of ophthalmology

Zip code

305-8575

Address

1-1-1 Tennoudai, Tsukuba, Ibaraki

TEL

029-853-3148

Email

yoshimis@md.tsukuba.ac.jp


Public contact

Name of contact person

1st name Tomoya
Middle name
Last name Murakami

Organization

University of Tsukuba

Division name

Department of ophthalmology

Zip code

305-8575

Address

1-1-1 Tennoudai, Tsukuba, Ibaraki

TEL

029-853-3148

Homepage URL


Email

murakami-tuk@umin.ac.jp


Sponsor or person

Institute

University of Tsukuba

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

Tsukuba Clinical Research and Development Organization

Address

2-1-1 Amakubo, Tsukuba, Ibaraki

Tel

029-853-3914

Email

t-credo.adm@un.tsukuba.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

2020 Year 08 Month 21 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

Main results already published

Date of protocol fixation

2020 Year 06 Month 24 Day

Date of IRB

2020 Year 06 Month 24 Day

Anticipated trial start date

2020 Year 08 Month 21 Day

Last follow-up date

2020 Year 11 Month 30 Day

Date of closure to data entry

2020 Year 12 Month 01 Day

Date trial data considered complete

2020 Year 12 Month 03 Day

Date analysis concluded

2020 Year 12 Month 05 Day


Other

Other related information

Retrospective observational study


Management information

Registered date

2020 Year 08 Month 20 Day

Last modified on

2022 Year 03 Month 23 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046706


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name