Centre For Clinical Research And Biostatistics (CCRB)

Back History

1 Unique Trial Number (assigned by CCRB)

CUHK_CCT00057

2 Trial Registration Date

2005-12-13

iRegistration Status

Retrospective

3 Secondary IDs

Not applicable

4 Source(s) of Funding

N/A

5 Primary Sponsor

Nil

6 Secondary Sponsor

Nil

Function

Please specify

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

i Name

Ms Joyce KUNG

ii Address

UEC, 3/F Hong Kong Eye Hospital, 147K Argyle St., Kln

iii Phone

3943 5813

iv Email

joycekung@cuhk.edu.hk

v Affiliation

Department of Ophthalmology and Visual Sciences

vi Country

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

i Name

Prof. Dennis SC Lam

ii Address

UEC, 3/F Hong Kong Eye Hospital, 147K Argyle St., Kln

iii Phone

3943 5813

iv Email

email dennislam_cu_res@cuhk.edu.hk

v Affiliation

Department of Ophthalmology and Visual Sciences

vi Country

9 Official Scientific Title of the Study

Identification of genes for high myopia

10 Public Title

Identification of genes for high myopia

i Public Title in Chinese 研究名稱

11 Short Title (Optional)

Not applicable

12 Countries of Recruitment

Hong Kong

13Research Ethic Review

i Has the study received appropriate ethics approval?

Yes

ii When is the approval date?

2004-02-28

iii Full Name of IRB/IEC

Please specify

iv IRB/IEC approval reference number

14 Medical Condition Being Studied

Eye Diseases

15Intervention

i Types of intervention

Other

Please specify

Nil

ii Description/ name of Intervention/article

Nil

iii Dosage form of the intervention

iv Dosage of the intervention

v Duration of the intervention

5 years

vi Frequency of the intervention

16Comparative Treatments

i Description/ name of comparative treatments

Nil

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

Inclusion criteria: Plan to carry out whole genome scan and linkage studies of 30 independent pedigrees of at least 3 generations, each with more than 10 members and 3 high myopia that we have recruited. None of these families have myopia associated disease such as Stickler's syndrome, Marfan syndrome and juvenile glaucoma.

ii Exclusion Criteria

Subjects with known or suspected medical disorders or ocular complications other than those described

iii Age Minimum

Nil

iv Age Maximum

Nil

v Gender

Both Male and Female

18 Study Type

Observational

19Study Design

i Randomization

Non-randomized

Please specify

ii Nature of control

Active

iii Degree of masking

Open label

If Single-blind, who will be masked?

iv Group Assignment

Single group

v Study Phase

Please specify

vi Study Objectives (Optional)

20 Anticipated trial start date

2004-07-01

21 Target Sample Size

1500

22 Recruitment Status

Recruiting

23 Primary Outcome

Advancing knowledge in basic molecular genetics.

24 Secondary Outcome

1. Affirm chromosomal loci linked to myopia. 2. Identify new myopia genes. 3. Reveal the frequencies of specific sequence alterations in the new putative myopia gene(s) in the local Chinese population. 4. Establish a basis to study interactive effects between environmental and genetic factors that contribute to myopia.

25Study Information/Publication

i Study Information/Publication Available?

No

ii Link to Study Information/Publication

26Last Update Date

2015-06-23

27 Primary Registry and Trial Identifying Number

ChiCTR-ONC-05000675

28 Date of Registration in Primary Registry

2010-05-04

Back History

Trial Detail