UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000011597
Receipt number R000013562
Scientific Title Fundus imaging using novel high resolution scannning LASER ophthalmoscope (SLO)
Date of disclosure of the study information 2013/08/30
Last modified on 2013/08/28 22:44:31

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Fundus imaging using novel high resolution scannning LASER ophthalmoscope (SLO)

Acronym

Fundus imaging using novel high resolution scannning LASER ophthalmoscope (SLO)

Scientific Title

Fundus imaging using novel high resolution scannning LASER ophthalmoscope (SLO)

Scientific Title:Acronym

Fundus imaging using novel high resolution scannning LASER ophthalmoscope (SLO)

Region

Japan


Condition

Condition

patients with:
macular disease (age-related macular degeneration, macular hole, macular pucker etc.),
diabetic retinopathy,
dyslipidemia,
hypertension,
systemic lupus erythematosus

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To take images of the human ocular fundus, and evaluate based on medical perspective.
To confirm for clinical condition grasp of a diagnosis of the primary disease and the illness of the primary disease effectively.
To confirm functions in discovery effectively that a ocular complication by the lifestyle related disease and the clinical views that ocular fundus.

Basic objectives2

Others

Basic objectives -Others

To confirm structural change from blood vessel morphological feature.
To confirm each characteristic and the difference of various cases.
To confirm time-dependent change of various cases.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

To take retinal images for patients by using the novel SLO equipment, and assess relationship between fundus images and various cases.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

To examine eligibility and take fundus images in a day.

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

Patient
1) Male or female older than 20 years-old
2) patients with:
macular disease (age-related macular degeneration, macular hole, macular pucker etc.),
diabetic retinopathy,
dyslipidemia,
hypertension,
systemic lupus erythematosus
3) Subjects who sign an informed consent form to participate in the clinical study

Key exclusion criteria

1) Having any side-effects (hypersensitivity, rised intraocular pressure etc.) against mydriatics
2) Revealed narrow angle by slit-lamp examination
3) When a doctor accepted the middle-class above-mentioned cataract
4) Subjects who a doctor in attendance declares ineligible for any reason

Target sample size

220


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Nagahisa Yoshimura

Organization

Kyoto University Graduate School of Medicine

Division name

Ophthalmology & Visual Sciences

Zip code


Address

54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto, JAPAN

TEL

075-751-3248

Email

nagaeye@kuhp.kyoto-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Akihito Uji

Organization

Kyoto University Graduate School of Medicine

Division name

Ophthalmology & Visual Sciences

Zip code


Address

54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto, JAPAN

TEL

075-751-3248

Homepage URL


Email

akihito1@kuhp.kyoto-u.ac.jp


Sponsor or person

Institute

Department of Ophthalmology & Visual Sciences, Kyoto University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Ministry of Education, Culture, Sports, Science and Technology (MEXT)

Organization

Division

Category of Funding Organization

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

2013 Year 08 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

Preinitiation

Date of protocol fixation

2012 Year 12 Month 21 Day

Date of IRB


Anticipated trial start date

2013 Year 09 Month 21 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2013 Year 08 Month 28 Day

Last modified on

2013 Year 08 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013562


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name