Centre For Clinical Research And Biostatistics (CCRB)

Back History

1 Unique Trial Number (assigned by CCRB)

CUHK_CCT00049

2 Trial Registration Date

2005-09-09

iRegistration Status

Retrospective

3 Secondary IDs

Nil

4 Source(s) of Funding

Nil

5 Primary Sponsor

n/a

6 Secondary Sponsor

n/a

Function

Please specify

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

i Name

Prof. Clement CY Tham

ii Address

Dept. of Ophthalmology & Visual Sciences, Hong Kong Eye Hospital

iii Phone

2762 3196

iv Email

clemtham@hkstar.com

v Affiliation

The Chinese University of Hong Kong

vi Country

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

i Name

Prof. Clement CY Tham

ii Address

Dept. of Ophthalmology & Visual Sciences, Hong Kong Eye Hospital

iii Phone

2762 3196

iv Email

clemtham@hkstar.com

v Affiliation

The Chinese University of Hong Kong

vi Country

9 Official Scientific Title of the Study

Glaucoma drainage device with and without adjunctive intra-bleb injection of triamcinolone acetonide: a randomized controlled trial.

10 Public Title

Glaucoma drainage device with and without adjunctive intra-bleb injection of triamcinolone acetonide: a randomized controlled trial.

i Public Title in Chinese 研究名稱

11 Short Title (Optional)

Nil

12 Countries of Recruitment

Hong Kong

13Research Ethic Review

i Has the study received appropriate ethics approval?

Yes

ii When is the approval date?

2005-03-24

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

Drug

Please specify

ii Description/ name of Intervention/article

adjunctive intra-bleb injection of triamcinolone acetonide

iii Dosage form of the intervention

iv Dosage of the intervention

v Duration of the intervention

5 minutes

vi Frequency of the intervention

16Comparative Treatments

i Description/ name of comparative treatments

No injection of triamcinolone acetonide

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 1. Eyes requiring glaucoma drainage device who had either Ü uncontrolled glaucoma despite previous trabeculectomy with adjunctive antimetabolite; Ü secondary glaucomas where routine trabeculectomy, with or without adjunctive antimetabolites, is unlikely to be successful, for example, active neovascular glaucoma, aniridia and glaucoma following traumatic anterior segment disruption. 2. Patient able and willing to give informed consent to participation in this study, and to glaucoma drainage device implantation.

ii Exclusion Criteria

Exclusion criteria 1. Single functional eye

iii Age Minimum

n / a

iv Age Maximum

n / a

v Gender

Both Male and Female

18 Study Type

Interventional

19Study Design

i Randomization

Randomized

Please specify

ii Nature of control

Placebo

iii Degree of masking

Open label

If Single-blind, who will be masked?

iv Group Assignment

Parallel

v Study Phase

Please specify

vi Study Objectives (Optional)

20 Anticipated trial start date

2005-03-24

21 Target Sample Size

20

22 Recruitment Status

Complete

23 Primary Outcome

IOP VA

24 Secondary Outcome

Number of IOP-lowering medications Change in visual field by automated perimetry (Humphrey¡¦s) Change in cup-to-disc ratio of the optic nerve head Rate of aqueous outflow by pneumatonometer measurements (for UCH patient) Anterior segment inflammation Bleb morphology Complication

25Study Information/Publication

i Study Information/Publication Available?

No

ii Link to Study Information/Publication

26Last Update Date

2009-11-24

27 Primary Registry and Trial Identifying Number

ChiCTR-TRC-09000744

28 Date of Registration in Primary Registry

2010-05-04

Back History

Trial Detail