Centre For Clinical Research And Biostatistics (CCRB)

Back History

1 Unique Trial Number (assigned by CCRB)

CUHK_CCT00412

2 Trial Registration Date

2014-05-14

iRegistration Status

Prospective

3 Secondary IDs

CRE-2014.051

4 Source(s) of Funding

Division funding

5 Primary Sponsor

Division of Cardiology, Department of Medicine & Therapeutics, Prince of Wales Hospital, CUHK

6 Secondary Sponsor

N/A

Function

Please specify

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

i Name

Ming LIU

ii Address

Division of Cardiology, Department of Medicine & Therapeutics, Prince of Wales Hospital, CUHK

iii Phone

(852) 26323840

iv Email

minglau@cuhk.edu.hk

v Affiliation

Division of Cardiology, Department of Medicine & Therapeutics, Prince of Wales Hospital, CUHK

vi Country

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

i Name

Prof. Chuek-Man Yu

ii Address

Division of Cardiology, Department of Medicine & Therapeutics, Prince of Wales Hospital, CUHK

iii Phone

(852)26323594

iv Email

cmyu@cuhk.edu.hk

v Affiliation

Division of Cardiology, Department of Medicine & Therapeutics, Prince of Wales Hospital, CUHK

vi Country

9 Official Scientific Title of the Study

Acute Coronary Syndrome Registry: Review of Treatment and Outcome in Last 10 Years

10 Public Title

Acute Coronary Syndrome Registry: Review of Treatment and Outcome in Last 10 Years

i Public Title in Chinese 研究名稱

急性冠狀動脈綜合症註冊研究：近10年治療和結果回顧

11 Short Title (Optional)

N/A

12 Countries of Recruitment

Hong Kong

13Research 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

Acute Coronary Syndrome

15Intervention

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

16Comparative 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

17Key Inclusion and Exclusion Criteria

i Inclusion Criteria

Adult patients who admitted to Prince of Wales Hospital due to Acute Coronary Syndrome (ACS) from 01-01-2004 to 31-12-2013

ii Exclusion Criteria

ACS Patients with age < or =18 years old

iii Age Minimum

19

iv Age Maximum

999

v Gender

Both Male and Female

18 Study Type

Observational

19Study Design

i Randomization

Not Applicable

Please specify

ii Nature of control

Not Applicable

iii Degree of masking

Not Applicable

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

Unknown

23 Primary Outcome

Compare the treatment differences for ACS patients over the 10 years

24 Secondary Outcome

Compare the outcome differences for ACS patients over the 10 years

25Study Information/Publication

i Study Information/Publication Available?

No

ii Link to Study Information/Publication

26Last Update Date

2015-06-15

27 Primary Registry and Trial Identifying Number

ChiCTR-OO-14004663

28 Date of Registration in Primary Registry

2014-05-18

Back History

Trial Detail