UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000005832 |
|---|---|
| Receipt number | R000006882 |
| Scientific Title | Ocular biometry before and after glaucoma surgery |
| Date of disclosure of the study information | 2011/10/01 |
| Last modified on | 2011/12/06 09:57:52 |
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Basic information
Public title
Ocular biometry before and after glaucoma surgery
Acronym
Ocular biometry before and after glaucoma surgery
Scientific Title
Ocular biometry before and after glaucoma surgery
Scientific Title:Acronym
Ocular biometry before and after glaucoma surgery
Region
| Japan |
Condition
Condition
glaucoma
Classification by specialty
| Ophthalmology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To comprehensively evaluate the impact of glaucoma surgery on ocular geometry by performing anterior and posterior ocular imaging before and after glaucoma surgery.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
intraocular pressure, visual acuity, refraction, corneal radius, anterior chamber depth, corneal epithelial cell count, central corneal thickness, higher order ablation, retinal thickness, nerve fiber layer thickness, choroidal thickness, axial length
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
| 100 | years-old | > |
Gender
Male and Female
Key inclusion criteria
Patients with medically uncontrollable glaucoma scheduled for glaucoma surgery or combined glaucoma and catract surgery.
Key exclusion criteria
Patients with other severe ocular disorders. Patients with no light perception. Patients under 20 years old.
Target sample size
150
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Atsuya Miki |
Organization
Osaka University Graduate School of Medicine
Division name
Department of Ophthalmology
Zip code
Address
2-2 Yamada-oka, Suita, Osaka
TEL
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name |
Organization
Osaka University Graduate School of Medicine
Division name
Department of Ophthalmology
Zip code
Address
2-2 Yamada-oka, Suita, Osaka
TEL
Homepage URL
Sponsor or person
Institute
Osaka University Graduate School of Medicine
Institute
Department
Personal name
Funding Source
Organization
Osaka University Graduate School of Medicine
Organization
Division
Category of Funding Organization
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
| 2011 | Year | 10 | 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
Enrolling by invitation
Date of protocol fixation
| 2011 | Year | 05 | Month | 24 | Day |
Date of IRB
Anticipated trial start date
| 2011 | Year | 06 | 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
Design: Prospective study
Assingment: None
Schedule: Ocular examination preoperatively and 1 month, 3 month, 6 month, 1 Year post operatively.
Management information
Registered date
| 2011 | Year | 06 | Month | 22 | Day |
Last modified on
| 2011 | Year | 12 | Month | 06 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000006882
