UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000008539
Receipt number R000009645
Scientific Title Evaluation for drug combination of antihypertensive agent and lipid-lowering agent in patients with hypertension and dyslipidemia
Date of disclosure of the study information 2012/07/26
Last modified on 2021/05/07 10:15:09

* 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

Evaluation for drug combination of antihypertensive agent and lipid-lowering agent in patients with hypertension and dyslipidemia

Acronym

Evaluation for drug combination of antihypertensive agent and lipid-lowering agent in patients with hypertension and dyslipidemia

Scientific Title

Evaluation for drug combination of antihypertensive agent and lipid-lowering agent in patients with hypertension and dyslipidemia

Scientific Title:Acronym

Evaluation for drug combination of antihypertensive agent and lipid-lowering agent in patients with hypertension and dyslipidemia

Region

Japan


Condition

Condition

Hypertension and dyslipidemia

Classification by specialty

Medicine in general Cardiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Evaluation for drug combination of antihypertensive agent and lipid-lowering agent

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

Blood pressure and LDL-Cholesterol

Key secondary outcomes



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

Intervention by Drug combination therapy

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients during current therapy with antihypertensive agent`amlodipine` and lipid-lowering agent`statin` tehrapy are eligible.

Key exclusion criteria

Patients without written imformed consent

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Ryuutaro Yamaguchi

Organization

Saitama Medical Center, Saitama Medical University

Division name

Division of Cardiology

Zip code


Address

1981 Kamoda, Kawagoe, Saitama

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Saitama Medical Center, Saitama Medical University

Division name

Division of Cardiology

Zip code


Address


TEL

049-228-3587

Homepage URL


Email



Sponsor or person

Institute

Saitama Medical Center, Saitama Medical University

Institute

Department

Personal name



Funding Source

Organization

Saitama Medical Center, Saitama Medical 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


Email



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 07 Month 26 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

Terminated

Date of protocol fixation

2012 Year 07 Month 05 Day

Date of IRB

2012 Year 07 Month 05 Day

Anticipated trial start date

2012 Year 08 Month 01 Day

Last follow-up date

2012 Year 08 Month 01 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 07 Month 26 Day

Last modified on

2021 Year 05 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000009645


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name