UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000054014
Receipt number R000059374
Scientific Title Cohort Study for Patients with Acute Chest Pain
Date of disclosure of the study information 2024/04/01
Last modified on 2024/03/30 05:21:26

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Basic information

Public title

Cohort Study for Patients with Acute Chest Pain

Acronym

Cohort Study for Patients with Acute Chest Pain

Scientific Title

Cohort Study for Patients with Acute Chest Pain

Scientific Title:Acronym

Cohort Study for Patients with Acute Chest Pain

Region

Japan


Condition

Condition

acute coronary syndrome

Classification by specialty

Medicine in general Cardiology Emergency medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Validation of the utility of Heart Score for acute chest pain cases suspected of acute coronary syndrome

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

death or acute coronary syndrome within 30 days

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

18 years-old <

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients presenting to the emergency department with acute chest pain and suspected acute coronary syndrome

Key exclusion criteria

age under 18 years old
obvious trauma
ST elevation acute myocardial infarction
shock

Target sample size

500


Research contact person

Name of lead principal investigator

1st name Mamoru
Middle name
Last name Toyofuku

Organization

Japanese Red Cross Wakayama Medical Center

Division name

Department of Cardiology

Zip code

640-8558

Address

4-20 Komatsubara-dori Wakayama City

TEL

073-422-4171

Email

matoyofuku-circ@umin.ac.jp


Public contact

Name of contact person

1st name Mamoru
Middle name
Last name Toyofuku

Organization

Japanese Red Cross Wakayama Medical Center

Division name

Department of Cardiology

Zip code

640-8558

Address

4-20 Komatsubara-dori Wakayama City

TEL

073-422-4171

Homepage URL


Email

matoyofuku-circ@umin.ac.jp


Sponsor or person

Institute

Japanese Red Cross Wakayama 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

Ethics Comitree, Japanese Red Cross Wakayama Medical Center

Address

4-20 Komatsubara-dori Wakayama City

Tel

073-422-4171

Email

0112sin@wakayama-med.jrc.or.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

2024 Year 04 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

Enrolling by invitation

Date of protocol fixation

2023 Year 04 Month 01 Day

Date of IRB

2023 Year 09 Month 12 Day

Anticipated trial start date

2023 Year 04 Month 01 Day

Last follow-up date

2024 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Prospective single center registry of tertiary educational hospital to validate the Heart Pathway for the diagnosis and risk stratification of non-ST elevation acute coronary syndrome at emergency department(ED).
Measurements and end point; HEART score consists of five components of the history, electrocardiogram, age, risk factors, and troponin. Each component can be scored with zero, one or two points, depending on the extent of the abnormality. For patients with low risk heart score and negative troponin results including serial measurements, the HEART pathway recommends discharge from the ED without further testing. The endpoint was the composite of death, myocardial infarction, or coronary artery revascularization within 30 days.


Management information

Registered date

2024 Year 03 Month 30 Day

Last modified on

2024 Year 03 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000059374


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name