Centre For Clinical Research And Biostatistics (CCRB)

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1 Unique Trial Number (assigned by CCRB)

CUHK_CCT00411

2 Trial Registration Date

2014-05-14

i Registration Status

Prospective

3 Secondary IDs

CRE-2014.050

4 Source(s) of Funding

Division funding

5 Primary Sponsor

Division of Cardiology, Department of Medicine & Therapeutics, CUHK

6 Secondary Sponsor

N/A

Function

Please specify

7 Responsible Contact Person (public contact person for patients interested in participating)

i Name

Ming LIU

ii Address

Division of Cardiology, Department of Medicine & Therapeutics, CUHK

iii Phone

(852) 26323840

iv Email

minglau@cuhk.edu.hk

v Affiliation

Division of Cardiology, Department of Medicine & Therapeutics, CUHK

vi Country

8 Research Contact Person (person to contact for scientific inquiries)

i Name

Prof. Cheuk-Man Yu

ii Address

Division of Cardiology, Department of Medicine & Therapeutics, CUHK

iii Phone

(852)26323594

iv Email

cmyu@cuhk.edu.hk

v Affiliation

Division of Cardiology, Department of Medicine & Therapeutics, CUHK

vi Country

9 Official Scientific Title of the Study

Heart Failure Registry:Review of Treatment and Outcome in Last 10 Years

10 Public Title

Heart Failure Registry:Review of Treatment and Outcome in Last 10 Years

i Public Title in Chinese 研究名稱

心力衰竭註冊研究：近10年治療和結果回顧

11 Short Title (Optional)

N/A

12 Countries of Recruitment

Hong Kong

13 Research Ethic Review

i Has the study received appropriate ethics approval?

Yes

ii When is the approval date?

2014-03-11

iii Full Name of IRB/IEC

Please specify

iv IRB/IEC approval reference number

14 Medical Condition Being Studied

Heart Failure

15 Intervention

i Types of intervention

Other

Please specify

No intervention

ii Description/ name of Intervention/article

No intervention

iii Dosage form of the intervention

iv Dosage of the intervention

v Duration of the intervention

No intervention

vi Frequency of the intervention

16 Comparative Treatments

i Description/ name of comparative treatments

No intervention

ii Dosage form of the comparative treatments

iii Dosage of the comparative treatments

iv Duration of the comparative treatments

v Frequency of the comparative treatments

17 Key Inclusion and Exclusion Criteria

i Inclusion Criteria

Adult patients who are newly admitted to Prince of Walse Hospital due to heart faliure from 01-01-2004 to 31-12-2013

ii Exclusion Criteria

HF patients with age< or =18 years old

iii Age Minimum

19

iv Age Maximum

N/A

v Gender

Both Male and Female

18 Study Type

Observational

19 Study Design

i Randomization

Not Applicable

Please specify

ii Nature of control

Not Applicable

iii Degree of masking

Open label

If Single-blind, who will be masked?

iv Group Assignment

Not Applicable

v Study Phase

Please specify

vi Study Objectives (Optional)

20 Anticipated trial start date

2014-06-16

21 Target Sample Size

5000

22 Recruitment Status

Not Yet Recruiting

23 Primary Outcome

Treatment differences for CHF patients over 10 years

24 Secondary Outcome

Outcome differences for CHF patients over 10 years

25 Study Information/Publication

i Study Information/Publication Available?

No

ii Link to Study Information/Publication

26 Last Update Date

2015-06-04

27 Primary Registry and Trial Identifying Number

28 Date of Registration in Primary Registry

* Legacy Fields

i Recruitment Information Available?

Yes

ii Link to Recruitment Information

N/A

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Trial History Detail on 2014-05-14