UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000018006
Receipt number R000020870
Scientific Title Urinary albumin excretion in heart failure with preserved ejection fraction: an interim analysis of the CHART 2 study
Date of disclosure of the study information 2015/06/22
Last modified on 2015/06/22 15:19:54

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Basic information

Public title

Urinary albumin excretion in heart failure with preserved ejection fraction: an interim analysis of the CHART 2 study

Acronym

The CHART-2 Study: Urinary albumin excretion in CHF.

Scientific Title

Urinary albumin excretion in heart failure with preserved ejection fraction: an interim analysis of the CHART 2 study

Scientific Title:Acronym

The CHART-2 Study: Urinary albumin excretion in CHF.

Region

Japan


Condition

Condition

Chronic Heart Failure

Classification by specialty

Medicine in general Cardiology Nephrology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Heart failure with preserved ejection fraction (HFpEF) is characterized by multiple co-morbidities, including chronic kidney disease that is one of the prognostic risks for these patients. This study was performed to evaluate the value of determination of albuminuria using a urine dipstick test (UDT), combined with estimated glomerular filtration rate (eGFR), for prediction of mortality in HFpEF.

Basic objectives2

Others

Basic objectives -Others

Heart failure with preserved ejection fraction (HFpEF) is characterized by multiple co-morbidities, including chronic kidney disease that is one of the prognostic risks for these patients. This study was performed to evaluate the value of determination of albuminuria using a urine dipstick test (UDT), combined with estimated glomerular filtration rate (eGFR), for prediction of mortality in HFpEF.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

background, therapy, prognosis

Key secondary outcomes



Base

Study type


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

Maneuver

Interventions/Control_1

Additional Blood Sampling (5mL)

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

Stage C/D HF

Key exclusion criteria

None

Target sample size

4735


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiroaki Shimokawa

Organization

Tohoku University Graduate School of Medicine

Division name

Department of Cardiovascular Medicine

Zip code


Address

1-1 Seiryo-machi, Aoba-ku, Sendai, Japan

TEL

+81-22-717-7153

Email

shimo@cardio.med.tohoku.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Yasuhiko Sakata

Organization

Tohoku University Graduate School of Medicine

Division name

Department of Cardiovascular Medicine

Zip code


Address

1-1 Seiryo-machi, Aoba-ku, Sendai, Japan

TEL

+81-22-717-7153

Homepage URL


Email

sakatayk@cardio.med.tohoku.ac.jp


Sponsor or person

Institute

Department of Cardiovascular Medicine and Department of Evidenced-Based Cardiovascular Medicine, Tohoku University Graduate School of Medicine,
Tohoku Heart Failure Association

Institute

Department

Personal name



Funding Source

Organization

Evidenced-based Cardiovascular Medicine, Tohoku 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


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

2015 Year 06 Month 22 Day


Related information

URL releasing protocol


Publication of results

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

Main results already published

Date of protocol fixation

2006 Year 06 Month 19 Day

Date of IRB


Anticipated trial start date

2006 Year 10 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 06 Month 22 Day

Last modified on

2015 Year 06 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020870


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name