UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000009209 |
|---|---|
| Receipt number | R000010809 |
| Scientific Title | The study of the effects of oral N/L-type calcium channel blocker cilnidipine on urinary excretions of albumin and podocyte in Japanese hypertensive patients. |
| Date of disclosure of the study information | 2012/10/29 |
| Last modified on | 2015/03/24 09:05:58 |
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Basic information
Public title
The study of the effects of oral N/L-type calcium channel blocker cilnidipine on urinary excretions of albumin and podocyte in Japanese hypertensive patients.
Acronym
The study of the effects of oral N/L-type calcium channel blocker cilnidipine on urinary excretions of albumin and podocyte in Japanese hypertensive patients.
Scientific Title
The study of the effects of oral N/L-type calcium channel blocker cilnidipine on urinary excretions of albumin and podocyte in Japanese hypertensive patients.
Scientific Title:Acronym
The study of the effects of oral N/L-type calcium channel blocker cilnidipine on urinary excretions of albumin and podocyte in Japanese hypertensive patients.
Region
| Japan |
Condition
Condition
hypertensive patients
Classification by specialty
| Endocrinology and Metabolism | Nephrology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To comparison of the effects of cilnidipine and the other CCBs on urinary excretions of albumin and podocyte in Japanese hypertensive patients.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Exploratory
Trial characteristics_2
Pragmatic
Developmental phase
Not applicable
Assessment
Primary outcomes
Changes in urinary excretions of albumin and podocyte between groups.
Key secondary outcomes
Changes in blood pressure control.
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
with cilnidipine for 24 weeks
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
Japanese hypertensive patients with renin-angiotensin system inhibitor and calcium antagonist (except for cilnidipine) for more than 3 months without requirement of adding other antihypertensive agents
SBP>130 mmHg, DBP>80 mmHg
Key exclusion criteria
acute illness or malignant tumors
drug allergy
with pregnant or breast feeding, or candidates with such situations
patients who are judged as inappropriate for inclusion by their physicians
Target sample size
50
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Masao Toyoda |
Organization
Tokai University School of Medicine
Division name
Division of Nephrology, Endocrinology and Metabolism
Zip code
Address
143 Shimokasuya, Isehara, Kanagawa 259-1193, JAPAN
TEL
0463-93-1121
m-toyoda@is.icc.u-tokai.ac.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Wakana Miura |
Organization
Tokai University School of Medicine
Division name
Division of Nephrology, Endocrinology and Metabolism
Zip code
Address
143 Shimokasuya, Isehara, Kanagawa 259-1193, JAPAN
TEL
0463-93-1121
Homepage URL
happy0897@gmail.com
Sponsor or person
Institute
Division of Nephrology, Endocrinology and Metabolism, Tokai University School of Medicine
Institute
Department
Personal name
Funding Source
Organization
Division of Nephrology, Endocrinology and Metabolism, Tokai University School of Medicine
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 | 10 | Month | 29 | 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
| 2010 | Year | 03 | Month | 31 | Day |
Date of IRB
Anticipated trial start date
| 2010 | Year | 04 | 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 | 10 | Month | 29 | Day |
Last modified on
| 2015 | Year | 03 | Month | 24 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000010809
