UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000009723
Receipt number R000011391
Scientific Title Study of relationship between OCT reflectivity and human blood components
Date of disclosure of the study information 2013/02/01
Last modified on 2023/01/15 18:24:14

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Basic information

Public title

Study of relationship between OCT reflectivity and human blood components

Acronym

Study of relationship between OCT reflectivity and human blood components

Scientific Title

Study of relationship between OCT reflectivity and human blood components

Scientific Title:Acronym

Study of relationship between OCT reflectivity and human blood components

Region

Japan


Condition

Condition

healthy subject or patients with macular edema

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To reveal relationship between OCT reflectivity and human blood components from healthy subject or patients with macular edema

Basic objectives2

Others

Basic objectives -Others

To assess the reproducibility of OCT reflectivity calculation

Trial characteristics_1

Exploratory

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

OCT reflectivity when blood sample was injected into the anterior chamber of the porcine eye
blood data of subject

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


Not applicable

Gender

Male and Female

Key inclusion criteria

Obtaining informed consent is possible that in patients with macular edema or healthy subjects

Does not matter the degree of visual acuity

Key exclusion criteria

A past history of treatment

A past history of eye surgery

Some difficulties to take picture due to cornea or lens opacity

Aphakia

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Taiji Sakamoto

Organization

Kagoshima University Graduate school od Medical and Dental Sciences

Division name

Ophthalmology

Zip code


Address

8-35-1 Sakuragaoka, Kagoshima, Japan

TEL

099-275-5402

Email

shou@m3.kufm.kagoshima-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Shozo Sonoda

Organization

Kagoshima University Graduate school od Medical and Dental Sciences

Division name

Ophthalmology

Zip code


Address

8-35-1 Sakuragaoka, Kagoshima, Japan

TEL

099-275-5402

Homepage URL


Email

shou@m3.kufm.kagoshima-u.ac.jp


Sponsor or person

Institute

Kagoshima University Graduate school od Medical and Dental Sciences

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


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 02 Month 01 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

2012 Year 12 Month 01 Day

Date of IRB

2012 Year 12 Month 01 Day

Anticipated trial start date

2013 Year 02 Month 01 Day

Last follow-up date

2015 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Prospective study


Management information

Registered date

2013 Year 01 Month 07 Day

Last modified on

2023 Year 01 Month 15 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000011391


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name