UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000018069 |
|---|---|
| Receipt number | R000020916 |
| Scientific Title | The clinical trial to examine the efficacy of the intravitreal injection of anti-VEGF antibody Bevacizumab(Avastin) for severe retinopathy of prematurity. |
| Date of disclosure of the study information | 2017/06/24 |
| Last modified on | 2015/06/24 15:00:28 |
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Basic information
Public title
The clinical trial to examine the efficacy of the intravitreal injection of anti-VEGF antibody Bevacizumab(Avastin) for severe retinopathy of prematurity.
Acronym
The clinical trial to examine the efficacy of the intravitreal injection of Bevacizumab for severe ROP.
Scientific Title
The clinical trial to examine the efficacy of the intravitreal injection of anti-VEGF antibody Bevacizumab(Avastin) for severe retinopathy of prematurity.
Scientific Title:Acronym
The clinical trial to examine the efficacy of the intravitreal injection of Bevacizumab for severe ROP.
Region
| Japan |
Condition
Condition
Retinopathy of prematurity
Classification by specialty
| Ophthalmology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
A purpose of this study is to prevent blindness from ROP and to examine the efficacy and safety of intravitreal bevacizumab for ROP.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Fundus examination
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
| Medicine |
Interventions/Control_1
Intravitreal Bevacizumab
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
| Not applicable |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
1)a premature baby
2)diagnosed as severe ROP
3)The patient in our hospital
4) The patient whose parents understand this study and the agreement in the document was provided.
Key exclusion criteria
1)The patient who judged inappropriate as a subject by pediatrician.
2)In addition, the patient who judged an examination responsibility (allotment) doctor to be inappropriate as a subject
Target sample size
4
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Shoji Kishi |
Organization
Gunma University Hospital
Division name
Department of Ophthalmology
Zip code
Address
3-39-15 Showa-machi, Maebashi-shi, Gunma
TEL
027-220-8338
shojikishi@gunma-u.ac.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Satomi Noda |
Organization
Gunma University Hospital
Division name
Department of Ophthalmology
Zip code
Address
3-39-15 Showa-machi, Maebashi-shi, Gunma
TEL
027-220-8338
Homepage URL
s-noda@gunma-u.ac.jp
Sponsor or person
Institute
Gunma University Hospital
Department of Ophthalmology
Institute
Department
Personal name
Funding Source
Organization
Gunma University Hospital
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
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
| 2017 | Year | 06 | Month | 24 | 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
| 2013 | Year | 06 | Month | 01 | Day |
Date of IRB
Anticipated trial start date
| 2013 | Year | 07 | Month | 01 | 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
| 2015 | Year | 06 | Month | 24 | Day |
Last modified on
| 2015 | Year | 06 | Month | 24 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020916
