UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000012094
Receipt number R000014132
Scientific Title Vitreous injection of anti vascular endothelium growth factor for macular edema.
Date of disclosure of the study information 2013/10/30
Last modified on 2023/08/16 23:51:54

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Basic information

Public title

Vitreous injection of anti vascular endothelium growth factor for macular edema.

Acronym

VEGF injection for macular edema

Scientific Title

Vitreous injection of anti vascular endothelium growth factor for macular edema.

Scientific Title:Acronym

VEGF injection for macular edema

Region

Japan


Condition

Condition

macular edema

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To determine usefulness of TER method for macular edema.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Visual acuity, intraocular pressure, anterior&posterior eye examination, visual function and morphology of retina.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Anti-VEGF addiministration using TER method.

Interventions/Control_2

Anti-VEGF addiministration using PRN method.

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

Macular edema with diabetes, retinal vein occulusion and uveites, those who obtained informed concent.

Key exclusion criteria

Those who under 20 years old, determined that not appropriatable by doctor and pregnant women.

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Masahiko
Middle name
Last name Sugimoto

Organization

Mie University Schoolof Medicine

Division name

Department of Ophthalmology

Zip code

514-8507

Address

2-174, Edobashi, Tsu, Mie, Japan, 514-8507

TEL

059-231-5027

Email

sugmochi@clin.medic.mie-u.ac.jp


Public contact

Name of contact person

1st name Masahiko
Middle name
Last name Sugimoto

Organization

Mie University Schoolof Medicine

Division name

Department of Ophthalmology

Zip code

514-8507

Address

2-174, Edobashi, Tsu, Mie, Japan, 514-8507

TEL

059-232-1111

Homepage URL


Email

sugmochi@clin.medic.mie-u.ac.jp


Sponsor or person

Institute

Mie University Schoolof Medicine

Institute

Department

Personal name



Funding Source

Organization

Mie University Schoolof Medicine

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

Mie University Schoolof Medicine

Address

2-174, Edobashi, Tsu, Mie, Japan

Tel

059-232-1111

Email

sugmochi@clin.medic.mie-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

2013 Year 10 Month 30 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

Completed

Date of protocol fixation

2013 Year 10 Month 11 Day

Date of IRB

2013 Year 10 Month 11 Day

Anticipated trial start date

2013 Year 11 Month 01 Day

Last follow-up date

2023 Year 03 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

2013 Year 10 Month 21 Day

Last modified on

2023 Year 08 Month 16 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000014132


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name