UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000003646
Receipt number R000004416
Scientific Title Intraocular dynamics of vascular endothelial growth factor levels in patients with neovascular glaucoma
Date of disclosure of the study information 2010/05/24
Last modified on 2011/11/27 16:13:25

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Basic information

Public title

Intraocular dynamics of vascular endothelial growth factor levels in patients with neovascular glaucoma

Acronym

Aqueous humor VEGF levels before and after intravitreal bevacizumab for neovascular glaucoma

Scientific Title

Intraocular dynamics of vascular endothelial growth factor levels in patients with neovascular glaucoma

Scientific Title:Acronym

Aqueous humor VEGF levels before and after intravitreal bevacizumab for neovascular glaucoma

Region

Japan


Condition

Condition

neovascular glaucoma

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the changes of aqueous humor VEGF levels before and after intravitreal bevacizumab and elucidate the optimal dosage of bevacizumab for treating neovascular glaucoma

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Changes of aqueous humor VEGF concentrations and intraocular pressures beore and after the high- and low-doses of intravitreal bevacizumab

Key secondary outcomes

Clinical evaluation of the changes in iris and angle neovascularization before and after the high- and low-doses of intravitreal bevacizumab


Base

Study type

Interventional


Study design

Basic design

expanded access

Randomization

Non-randomized

Randomization unit


Blinding

Open -but assessor(s) are blinded

Control

Dose comparison

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

intravitreal injection of 1.0-mg bevacizumab

Interventions/Control_2

intravitreal injection of 0.1-mg bevacizumab

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

Eyes with neovascular glaucoma scheduled for intravitreal injection of bevacizumab

Key exclusion criteria

Eyes with a past history of intravitreal pharmacotherapy

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Yusuke Oshima

Organization

Osaka University Medical School

Division name

Ophthalmology

Zip code


Address

2-2 Yamadaoka, Suita 5650871, Japan

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Osaka University Medical School

Division name

Ophthalmology

Zip code


Address


TEL

06-6879-3456

Homepage URL


Email



Sponsor or person

Institute

Osaka University Hospital, Department of Ophthalmology

Institute

Department

Personal name



Funding Source

Organization

Osaka University Medical School

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


Address


Tel


Email



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

2010 Year 05 Month 24 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications

http://www.liebertonline.com/doi/abs/10.1089/jop.2011.0059

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

2007 Year 12 Month 01 Day

Date of IRB


Anticipated trial start date

2008 Year 01 Month 01 Day

Last follow-up date

2009 Year 07 Month 01 Day

Date of closure to data entry

2009 Year 10 Month 01 Day

Date trial data considered complete

2009 Year 12 Month 01 Day

Date analysis concluded

2010 Year 03 Month 01 Day


Other

Other related information



Management information

Registered date

2010 Year 05 Month 21 Day

Last modified on

2011 Year 11 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000004416


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name