UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000014102
Receipt number R000016414
Scientific Title Fundus imaging and its association with prognosis in diabetic retinopathy
Date of disclosure of the study information 2014/05/28
Last modified on 2015/01/12 10:43:32

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Basic information

Public title

Fundus imaging and its association with prognosis in diabetic retinopathy

Acronym

Fundus imaging in diabetic retinopathy

Scientific Title

Fundus imaging and its association with prognosis in diabetic retinopathy

Scientific Title:Acronym

Fundus imaging in diabetic retinopathy

Region

Japan


Condition

Condition

diabetic retinopathy

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

to investigate the novel methods to assess the fundus imaging and to evaluate its usefulness as prognostic factors in diabetic retinopathy

Basic objectives2

Others

Basic objectives -Others

clinical observation study

Trial characteristics_1

Exploratory

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

qualitative and quantitative assessment of fundus imaging in diabetic retinopathy

Key secondary outcomes

association between prognosis and clinical parameters in fundus imaging


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


Not applicable

Gender

Male and Female

Key inclusion criteria

1)diabetic retinopathy

2)Patients who provided written informed consents to participate the study prior to enrollment

Key exclusion criteria

Other conditions considered inappropriate by attending physician

Patients with contraindication regarding the fundus imaging, including the allergy for fluorescein angiography

Target sample size

200


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Nagahisa Yoshimura

Organization

Graduate school of medicine and faculty of medicine Kyoto University

Division name

Department of ophthalmology and visual sciences

Zip code


Address

54 syougoinkawara-machi, sakyo-ku, Kyoto-city, Kyoto 606-8507, Japan

TEL

075-751-3248

Email

nagaeye@kuhp.kyoto-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Tomoaki Murakami

Organization

Graduate school of medicine and faculty of medicine Kyoto University

Division name

Department of ophthalmology and visual sciences

Zip code


Address

54 syougoinkawara-machi, sakyo-ku, Kyoto-city, Kyoto 606-8507, Japan

TEL

075-751-3248

Homepage URL


Email

mutomo@kuhp.kyoto-u.ac.jp


Sponsor or person

Institute

Department of ophthalmology and visual sciences, graduate school of medicine and faculty of medicine Kyoto University

Institute

Department

Personal name



Funding Source

Organization

none

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor

none

Name of secondary funder(s)

none


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

京都大学病院(京都府)


Other administrative information

Date of disclosure of the study information

2014 Year 05 Month 28 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

2014 Year 05 Month 28 Day

Date of IRB


Anticipated trial start date

2014 Year 07 Month 01 Day

Last follow-up date

2017 Year 06 Month 30 Day

Date of closure to data entry

2017 Year 06 Month 30 Day

Date trial data considered complete

2017 Year 10 Month 01 Day

Date analysis concluded

2017 Year 11 Month 01 Day


Other

Other related information

prospective study


Management information

Registered date

2014 Year 05 Month 28 Day

Last modified on

2015 Year 01 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000016414


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name