UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000037679
Receipt number R000042969
Scientific Title Effects of glaucoma on the therapeutic effects of anti-vascular endothelial growth factor agents on macular edema associated with retinal vein branch occlusion
Date of disclosure of the study information 2019/08/13
Last modified on 2019/08/13 20:37:48

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Basic information

Public title

Effects of glaucoma on the therapeutic effects of anti-vascular endothelial growth factor agents on macular edema associated with retinal vein branch occlusion

Acronym

Effects of glaucoma on on macular edema associated with retinal vein branch occlusion

Scientific Title

Effects of glaucoma on the therapeutic effects of anti-vascular endothelial growth factor agents on macular edema associated with retinal vein branch occlusion

Scientific Title:Acronym

Effects of glaucoma on on macular edema associated with retinal vein branch occlusion

Region

Japan


Condition

Condition

macular edema associated with retinal vein branch occlusion

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the effects of glaucoma on the therapeutic effects of anti-vascular endothelial growth factor inhibitors on macular edema associated with retinal vein branch occlusion

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The change of central retina thicknes

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

100 years-old >=

Gender

Male and Female

Key inclusion criteria

1)Visual disturbance due to center involved ME(evaluated using OCT)treated with anti-VEGF agents
2)BCVA(pre-treatment) is over 24 letters(20/320)
3)CRT>300 micro meter
4)Over 12 month followup after treatment.

Key exclusion criteria

1)Ocular diseases other than BRVO-ME
2)Severe general complications
3)Those who inappropriate

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Masahiko
Middle name
Last name Sugimoto

Organization

Mie University Graduate School of Medicine

Division name

Department of Ophthalmology

Zip code

514-8507

Address

2-174 Edobashi, Tsu, Mie, Japan

TEL

0592315027

Email

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


Public contact

Name of contact person

1st name Masahiko
Middle name Sugimoto
Last name Sugimoto

Organization

Mie University Graduate School of Medicine

Division name

Department of Ophthalmology

Zip code

514-8507

Address

2-174 Edobashi, Tsu, Mie, Japan

TEL

0592315027

Homepage URL


Email

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


Sponsor or person

Institute

Other

Institute

Department

Personal name



Funding Source

Organization

Other

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 Graduate School of Medicine

Address

2-174 Edobashi, Tsu, Mie, Japan

Tel

0592315027

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

2019 Year 08 Month 13 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

Enrolling by invitation

Date of protocol fixation

2019 Year 04 Month 25 Day

Date of IRB

2019 Year 04 Month 25 Day

Anticipated trial start date

2019 Year 04 Month 25 Day

Last follow-up date

2022 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

None.


Management information

Registered date

2019 Year 08 Month 13 Day

Last modified on

2019 Year 08 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042969


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name