UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000006005
Receipt number R000007106
Scientific Title The effects of olmesartan medoxomil on pulse wave velocity and oxidative stress in type2 diabetes mellitus-pulse wave velocity (baPWV, CAVI) subanalysis
Date of disclosure of the study information 2011/07/20
Last modified on 2020/01/24 11:15:40

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Basic information

Public title

The effects of olmesartan medoxomil on pulse wave velocity and oxidative stress in type2 diabetes mellitus-pulse wave velocity (baPWV, CAVI) subanalysis

Acronym

The effects of olmesartan medoxomil on pulse wave velocity and oxidative stress in type2 diabetes mellitus-pulse wave velocity (baPWV, CAVI) subanalysis

Scientific Title

The effects of olmesartan medoxomil on pulse wave velocity and oxidative stress in type2 diabetes mellitus-pulse wave velocity (baPWV, CAVI) subanalysis

Scientific Title:Acronym

The effects of olmesartan medoxomil on pulse wave velocity and oxidative stress in type2 diabetes mellitus-pulse wave velocity (baPWV, CAVI) subanalysis

Region

Japan


Condition

Condition

Type 2 Diabetes Mellitus

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate the effects of olmesartan medoxomil on pulse wave velocity (baPWV, CAVI) in type2 diabetes mellitus

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

To investigate the effects of olmesartan medoxomil on pulse wave velocity (baPWV, CAVI) in type2 diabetes mellitus

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

Duration24 weeks
Type 2 Diabetes Mellitus
Drug 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

30 years-old <=

Age-upper limit

80 years-old >

Gender

Male and Female

Key inclusion criteria

Patients who have systolic blood pressure 130mmHg and/or diastolic blood pressure in type 2 diabetes mellitus

Key exclusion criteria

patient who has the impairment of renal
function (Cr >2mg/dl)
patient who has malabsorption syndrome, the impairment of cerebral blood flow or epilepsy
patient who has hyperkalemia
patient who has severe cardiac, hepatic or pancreatic disorder
patient who has pregnant, nurses a baby or may get pregnant
patient who is unsuitable for this study (judged by a doctor)

Target sample size

10


Research contact person

Name of lead principal investigator

1st name Michio
Middle name
Last name Otsuki

Organization

Osaka University Graduate school of Medicine

Division name

Department of Metabolic Medicine

Zip code

565-0871

Address

2-2 Yamada-oka, Suita, Osaka, Japan

TEL

06-6879-3732

Email

otsuki@endmet.med.osaka-u.ac.jp


Public contact

Name of contact person

1st name Michio
Middle name
Last name Otsuki

Organization

Osaka University Graduate School of Medicine

Division name

Department of Metabolic Medicine

Zip code

565-0871

Address

2-2 Yamada-oka, Suita, Osaka, Japan

TEL

06-6879-3732

Homepage URL


Email

otsuki@endmet.med.osaka-u.ac.jp


Sponsor or person

Institute

Department of Metabolic Medicine
Osaka University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Department of Metabolic Medicine
Osaka University Graduate School of Medicine

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

Osaka University Clinical Research Review Committee

Address

2-15 Yamada-oka, Suita, Osaka, Japan

Tel

06-6879-5682

Email

rinri@hp-crc.med.osaka-u.ac.jp


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 07 Month 20 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

Completed

Date of protocol fixation

2011 Year 02 Month 10 Day

Date of IRB

2011 Year 02 Month 01 Day

Anticipated trial start date

2011 Year 02 Month 01 Day

Last follow-up date

2014 Year 06 Month 30 Day

Date of closure to data entry

2014 Year 12 Month 31 Day

Date trial data considered complete

2014 Year 12 Month 31 Day

Date analysis concluded

2016 Year 12 Month 31 Day


Other

Other related information



Management information

Registered date

2011 Year 07 Month 19 Day

Last modified on

2020 Year 01 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007106


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name