UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000007152 |
|---|---|
| Receipt number | R000008422 |
| Scientific Title | The Efficacy of pretretment with ocular-hypotensive agants on the patients with cataract surgery |
| Date of disclosure of the study information | 2012/02/14 |
| Last modified on | 2019/08/07 12:04:23 |
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Basic information
Public title
The Efficacy of pretretment with ocular-hypotensive agants on the patients with cataract surgery
Acronym
The Efficacy of ocular-hypotensive agants on post cataract surgery
Scientific Title
The Efficacy of pretretment with ocular-hypotensive agants on the patients with cataract surgery
Scientific Title:Acronym
The Efficacy of ocular-hypotensive agants on post cataract surgery
Region
| Japan |
Condition
Condition
The patients with cataract surgery
Classification by specialty
| Ophthalmology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To inevstigate whether pretretment of ocular-hypotensive agents contribute the post operatinve intraocular pressure
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Not applicable
Assessment
Primary outcomes
intraocular pressure
Key secondary outcomes
Change of intraocular pressure
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
No treatment
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Treatment
Type of intervention
| Medicine |
Interventions/Control_1
ocular hypotensive agents
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
1)Patients who accepted catract-surgery
2)Regardless of sex.
3)Aged 20 years or more.
4)Outpatients.
"
Key exclusion criteria
1)Patinets who with a history of allergy (i.e. hypersensitivity) to the drugs to be used during the study period.
2)Patinets who need wearing contact lenses during the study period.
"
Target sample size
100
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Takashi Kanamoto |
Organization
Hiroshima University
Division name
Depertment of Ophthalomology
Zip code
Address
1-2-3, Kasumi, Minami-ku, Hiroshima
TEL
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name |
Organization
Hiroshima University
Division name
Depertment of Ophthalomology
Zip code
Address
1-2-3, Kasumi, Minami-ku, Hiroshima
TEL
Homepage URL
Sponsor or person
Institute
Depertment of Ophthalomology, Hiroshima University
Institute
Department
Personal name
Funding Source
Organization
Depertment of Ophthalomology, Hiroshima 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
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
| 2012 | Year | 02 | Month | 14 | 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 | 14 | Day |
Date of IRB
| 2012 | Year | 12 | Month | 14 | Day |
Anticipated trial start date
| 2012 | Year | 12 | Month | 14 | Day |
Last follow-up date
| 2015 | Year | 03 | Month | 30 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2012 | Year | 01 | Month | 27 | Day |
Last modified on
| 2019 | Year | 08 | Month | 07 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000008422
