UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000038007
Receipt number R000043325
Scientific Title Analysis of morphological characteristics of choroidal structure in central serous chorioretinopathy.
Date of disclosure of the study information 2019/10/01
Last modified on 2022/03/17 01:27:15

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Basic information

Public title

Analysis of morphological characteristics of choroidal structure in central serous chorioretinopathy.

Acronym

Choroidal structure in central serous chorioretinopathy.

Scientific Title

Analysis of morphological characteristics of choroidal structure in central serous chorioretinopathy.

Scientific Title:Acronym

Choroidal structure in central serous chorioretinopathy.

Region

Japan


Condition

Condition

central serous chorioretinopathy

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The charactaristics of choroidal structure of central serous chorioretinopathy are observed in detail by multiple ophthalmic examinations such as optical coherence tomography and optical coherence tomography angiography.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Sex, age, visual acuity, visual field, refraction, ocular axial length, fundus observation,Optical coherence tomography, optical coherence tomography angiography, fundus photograph, fluorescence fundus angiography, slit lamp microscopy, duration of disease, current medical history, past history, family history

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

Treatment naive central serous chorioretinopathy

Key exclusion criteria

Patients who pre- and post-operative imaging examinations cannot be performed.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name jun
Middle name
Last name takeuchi

Organization

Nagoya University Hospital

Division name

Department of Ophthalmology

Zip code

466-0065

Address

65 Tsurumai-cho, Showa-ku, Nagoya

TEL

052-744-2275

Email

takeuchi.jun@med.nagoya-u.ac.jp


Public contact

Name of contact person

1st name takeuchi
Middle name
Last name jun

Organization

Nagoya University Hospital

Division name

Department of Ophthalmology

Zip code

466-0065

Address

65 Tsurumai-cho, Showa-ku, Nagoya

TEL

052-744-2275

Homepage URL


Email

takeuchi.jun@med.nagoya-u.ac.jp


Sponsor or person

Institute

Nagoya University

Institute

Department

Personal name



Funding Source

Organization

Nagoya University

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

Institutional Review Board of Nagoya University Graduate School of Medicine

Address

65 Tsurumai-cho, Showa-ku, Nagoya

Tel

052-744-2275

Email

ethics@med.nagoya-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 10 Month 01 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled

20

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

2019 Year 10 Month 01 Day

Date of IRB

2019 Year 11 Month 06 Day

Anticipated trial start date

2020 Year 10 Month 01 Day

Last follow-up date

2023 Year 06 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

nothing


Management information

Registered date

2019 Year 09 Month 13 Day

Last modified on

2022 Year 03 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000043325


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name