UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000005396 |
|---|---|
| Receipt number | R000006402 |
| Scientific Title | Safety and effectiveness of selective retina therapy (SRT) for central serous chorioretinopathy |
| Date of disclosure of the study information | 2011/05/01 |
| Last modified on | 2019/10/22 20:20:12 |
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Basic information
Public title
Safety and effectiveness of selective retina therapy (SRT) for central serous chorioretinopathy
Acronym
Safety and effectiveness of SRT for CSCR
Scientific Title
Safety and effectiveness of selective retina therapy (SRT) for central serous chorioretinopathy
Scientific Title:Acronym
Safety and effectiveness of SRT for CSCR
Region
| Japan |
Condition
Condition
central serous chorioretinopathy
Classification by specialty
| Ophthalmology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Safety and effectiveness of selective retina therapy (SRT) for central serous chorioretinopathy
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
observation of optic coherence tomography
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
Treatment
Type of intervention
| Device,equipment |
Interventions/Control_1
methods:
After local anesthesia with Benoxil ophthalmic solution, we irradiate SRT laser for the lesion.
periodical evaluation:
Three months after first therapy, we retreat if the treatment is inadequate. We will make a follow-up one year after the first treatment.
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
patients with central serous chorioretinopathy caused subjective symptoms such as central scotoma, metamorphopsia and central visual loss
Key exclusion criteria
ophthalmic exclusion criteria:
patients who had inflammation within the eye
systemic exclusion criteria:
people who had systemic inflammatory disease, hemorrhagic diathesis or anticoagulant therapy, untreated hypertension or diabetes mellitus. peple who is pregnant or at risk of becoming pregnant.
Target sample size
10
Research contact person
Name of lead principal investigator
| 1st name | Kunihiko |
| Middle name | |
| Last name | Shiraki |
Organization
Osaka City University, Graduate School of Medicine, Department of Ophthalmology and Visual sciences
Division name
Ophthalmology
Zip code
545-8585
Address
1-4-3, Asahi-machi, Abenoku, Osaka-shi, Japan
TEL
06-6645-3867
manabun@msic.med.osaka-cu.ac.jp
Public contact
Name of contact person
| 1st name | Manabu |
| Middle name | |
| Last name | Yamamoto |
Organization
Osaka City University, Graduate School of Medicine, Department of Ophthalmology and Visual sciences
Division name
Ophthalmology
Zip code
545-8585
Address
1-4-3, Asahi-machi, Abenoku, Osaka-shi, Japan
TEL
06-6645-3867
Homepage URL
manabun@msic.med.osaka-cu.ac.jp
Sponsor or person
Institute
Osaka City University, Graduate School of Medicine, Department of Ophthalmology and Visual 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
Osaka City University Hospital Certified Review Board
Address
1-2-7-601, Asahi-machi, Abeno-ku, Osaka, Japan
Tel
06-6645-3456
ethics@med.osaka-cu.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
| 2011 | Year | 05 | Month | 01 | Day |
Related information
URL releasing protocol
Publication of results
Partially published
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
| 2011 | Year | 04 | Month | 01 | Day |
Date of IRB
| 2011 | Year | 03 | Month | 18 | Day |
Anticipated trial start date
| 2011 | Year | 06 | Month | 01 | Day |
Last follow-up date
| 2013 | Year | 12 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2011 | Year | 04 | Month | 07 | Day |
Last modified on
| 2019 | Year | 10 | Month | 22 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000006402
| Research Plan | |
|---|---|
| Registered date | File name |
| Research case data specifications | |
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| Registered date | File name |
| Research case data | |
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| Registered date | File name |
