UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000008577 |
|---|---|
| Receipt number | R000010076 |
| Scientific Title | Evaluation for Efficacy and Safety of Azilsartan in Patients with Hypertension |
| Date of disclosure of the study information | 2012/08/01 |
| Last modified on | 2014/12/08 15:43:48 |
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Basic information
Public title
Evaluation for Efficacy and Safety of Azilsartan in Patients with Hypertension
Acronym
Azilsartan in Hyperetnsives
Scientific Title
Evaluation for Efficacy and Safety of Azilsartan in Patients with Hypertension
Scientific Title:Acronym
Azilsartan in Hyperetnsives
Region
| Japan |
Condition
Condition
Essential Hypertension
Classification by specialty
| Medicine in general | Cardiology | Endocrinology and Metabolism |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To elucidate efficacy and safety of azilsartan in hypertensives
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
blood pressure
Key secondary outcomes
albuminuria, BNP
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
azilsartan
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
| 90 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
essential hypertensives
Key exclusion criteria
(1) past history of adverse reaction for azilsartan
(2) pregnant female or women suspected of being pregnant
(3) advanced renal insufficiency
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Ken-ichi Aihara |
Organization
The University of Tokushima, Graduate School of Health Biosciences
Division name
Medicine and Bioregulatory Sciences
Zip code
Address
3-18-15 Kuramoto-cho Tokushima
TEL
088-633-7120
aihara@tokushima-u.ac.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Ken-ichi Aihara |
Organization
The University of Tokushima, Graduate School of Health Biosciences
Division name
Medicine and Bioregulatory Sciences
Zip code
Address
3-18-15 Kuramoto-cho Tokushima
TEL
088-633-7120
Homepage URL
aihara@tokuhsima-u.ac.jp
Sponsor or person
Institute
Department of Medicine and Bioregulatory SciencesThe University of Tokushima, Graduate School of Health Biosciences
Institute
Department
Personal name
Funding Source
Organization
Department of Medicine and Bioregulatory SciencesThe University of Tokushima, Graduate School of Health Biosciences
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 | 08 | 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
Open public recruiting
Date of protocol fixation
| 2012 | Year | 07 | Month | 30 | Day |
Date of IRB
Anticipated trial start date
| 2012 | Year | 09 | 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
| 2012 | Year | 07 | Month | 31 | Day |
Last modified on
| 2014 | Year | 12 | Month | 08 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000010076
