UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000010161
Receipt number R000011899
Scientific Title Observational cohort study of acute heart failure in Yokohama, Yokohama Acute Heart Failure (YAHF) registry
Date of disclosure of the study information 2013/03/05
Last modified on 2014/11/05 08:10:46

* 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

Observational cohort study of acute heart failure in Yokohama, Yokohama Acute Heart Failure (YAHF) registry

Acronym

Yokohama Acute Heart Failure registry

Scientific Title

Observational cohort study of acute heart failure in Yokohama, Yokohama Acute Heart Failure (YAHF) registry

Scientific Title:Acronym

Yokohama Acute Heart Failure registry

Region

Japan


Condition

Condition

Acute heart failure

Classification by specialty

Medicine in general Cardiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To clarify the background, pathophysiology, epidemiology, therapy, and prognosis of acute heart failure.

Basic objectives2

Others

Basic objectives -Others

To clarify the background, pathophysiology(especially to verify the hypothesis that acute change in hemoglobin correlates heart failure profile: e.g. acute pulmonary edema, and that hypercapnia at admission is associated with the mode of admission and acute airway management), epidemiology, therapy, and prognosis of acute heart failure.

Trial characteristics_1

Confirmatory

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

Pathological, therapeutical, and prognostic parameters. (detailed outcome for above-mentioned hypothesis: acute changes in hemoglobin levels in each subgroups of heart failure (e.g. patients with or without acute pulmonary edema ), and mode of airway management in each subgroups of those with or without hypercapnia).

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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

Patients who met Framingham criteria.

Key exclusion criteria

None

Target sample size

450


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Masaaki Konishi

Organization

Yokohama City University Medical Center

Division name

Division of Cardiology

Zip code


Address

4-57 Urafune-cho, Minami-ku, Yokohama

TEL

045-261-5656

Email

m_koni@yokohama-cu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Masaaki Konishi

Organization

Yokohama City University Medical Center

Division name

Division of Cardiology

Zip code


Address

4-57 Urafune-cho, Minami-ku, Yokohama

TEL

045-253-5362

Homepage URL


Email

m_koni@yokohama-cu.ac.jp


Sponsor or person

Institute

Yokohama City University Medical Center

Institute

Department

Personal name



Funding Source

Organization

None

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

2013 Year 03 Month 05 Day


Related information

URL releasing protocol


Publication of results

Partially published


Result

URL related to results and publications

https://www.jstage.jst.go.jp/article/circj/78/4/78_CJ-13-1163/_pdf

Number of participants that the trial has enrolled


Results

Published in
https://www.jstage.jst.go.jp/article/circj/78/4/78_CJ-13-1163/_pdf

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

2009 Year 12 Month 01 Day

Date of IRB


Anticipated trial start date

2010 Year 01 Month 01 Day

Last follow-up date

2014 Year 12 Month 31 Day

Date of closure to data entry

2015 Year 12 Month 31 Day

Date trial data considered complete

2016 Year 12 Month 31 Day

Date analysis concluded

2017 Year 12 Month 31 Day


Other

Other related information

Patients enrollment ended by Dec. 2011. Only data at admission and during hospitalization are now analyzed.


Management information

Registered date

2013 Year 03 Month 04 Day

Last modified on

2014 Year 11 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000011899


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name