UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000018611 |
|---|---|
| Receipt number | R000021538 |
| Scientific Title | effect for sympathetic nerve activity of statin for heart failure with preserved ejection fraction |
| Date of disclosure of the study information | 2015/09/01 |
| Last modified on | 2015/08/09 17:31:35 |
* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments
Basic information
Public title
effect for sympathetic nerve activity of statin for heart failure with preserved ejection fraction
Acronym
effect for sympathetic nerve activity of statin for heart failure with preserved ejection fraction
Scientific Title
effect for sympathetic nerve activity of statin for heart failure with preserved ejection fraction
Scientific Title:Acronym
effect for sympathetic nerve activity of statin for heart failure with preserved ejection fraction
Region
| Japan |
Condition
Condition
chronic heart failure with preserved ejection fraction
Classification by specialty
| Cardiology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
investigation of sympathetic nerve of statin for HFpEF
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
regulation of muscle sympathetic nerve activity
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Medicine |
Interventions/Control_1
prescribe atrovastatin
Interventions/Control_2
prescribe lovastatin
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
1) chronic heart failure with preserved EF( >40%)
2) dyslipidemia
Key exclusion criteria
1) stroke
2) AMI within 3 months
3) ACS
4) IP
5) severe valvular desease or shunt desease
6) chronic kidney desease
7)chronic Af
8) DM
9) secondary hypertension
Target sample size
20
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Shuichi Kaneko |
Organization
Kanazawa University
Division name
departmento of desease control and homeostasis
Zip code
Address
13-1, Takara-machi, Kanazawa, 920-8641, Japan
TEL
076-265-2000
hidekitokuhisa@yahoo.co.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | hideki tokuhisa |
Organization
kanazawa university
Division name
department of desease control and homeostasis
Zip code
Address
13-1, Takara-machi, Kanazawa, K
TEL
090-2379-7809
Homepage URL
hidekitokuhisa@yahoo.co.jp
Sponsor or person
Institute
Kanazawa university
Institute
Department
Personal name
Funding Source
Organization
Kanazawa university
Organization
Division
Category of Funding Organization
Other
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
| 2015 | Year | 09 | 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
Preinitiation
Date of protocol fixation
| 2015 | Year | 07 | Month | 02 | Day |
Date of IRB
Anticipated trial start date
| 2015 | 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
| 2015 | Year | 08 | Month | 09 | Day |
Last modified on
| 2015 | Year | 08 | Month | 09 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000021538
