Centre For Clinical Research And Biostatistics (CCRB)

Back History

1 Unique Trial Number (assigned by CCRB)

CUHK_CCT00156

2 Trial Registration Date

2008-02-15

i Registration Status

Prospective

3 Secondary IDs

Not applicable

4 Source(s) of Funding

N/A

5 Primary Sponsor

Nil

6 Secondary Sponsor

Nil

Function

Please specify

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

i Name

Miss Joyce Kung

ii Address

3/F, Hong Kong Eye Hospital, 147K Argyle Street, Kowloon

iii Phone

27623134

iv Email

joycekung@cuhk.edu.hk

v Affiliation

Department of Ophthalmology & Visual Sciences, The Chinese University of Hong Kong

vi Country

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

i Name

Prof. Dennis SC Lam

ii Address

3/F, Hong Kong Eye Hospital, 147K Argyle Street, Kowloon.

iii Phone

27623134

iv Email

dennislam_cu_res@cuhk.edu.hk

v Affiliation

Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong

vi Country

9 Official Scientific Title of the Study

Intravitreal injection of Bevacizumab (Avastin®) as an adjunctive therapy of pterygium surgery to prevent recurrence: A pilot study

10 Public Title

Intravitreal injection of Bevacizumab (Avastin®) as an adjunctive therapy of pterygium surgery to prevent recurrence: A pilot study

i Public Title in Chinese 研究名稱

11 Short Title (Optional)

Not applicable

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?

2008-01-31

iii Full Name of IRB/IEC

Please specify

iv IRB/IEC approval reference number

14 Medical Condition Being Studied

pterygium

15 Intervention

i Types of intervention

Procedure

Please specify

ii Description/ name of Intervention/article

Intravitreal injection of Bevacizumab (Avastin®) after surgical excision of pterygium

iii Dosage form of the intervention

iv Dosage of the intervention

v Duration of the intervention

one injection immediately after surgical excision of pterygium

vi Frequency of the intervention

16 Comparative Treatments

i Description/ name of comparative treatments

There is no comparative treatment as this is a pilot study. We will observe the recurrence rate of pterygium being treated with adjunctive intravitreal Avastin injection and design a randomized controlled trial in the future.

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

Inclusion criteria: 1. Age 18 years or above 2. Eye with single-head primary or secondary pterygium 3. Patient able and willing to give informed consent to the pterygium surgery with intravitreal injections of bevacizumab

ii Exclusion Criteria

Exclusion criteria: 1. Single functional eye 2. Pregnant patients 3. Use of anticoagulants or antiplatelet therapy other than aspirin / NSAID within 14 days of surgery.

iii Age Minimum

18

iv Age Maximum

None set

v Gender

Both Male and Female

18 Study Type

Interventional

19 Study Design

i Randomization

Non-randomized

Please specify

ii Nature of control

Uncontrolled

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

2008-03-01

21 Target Sample Size

50 eyes

22 Recruitment Status

Complete

23 Primary Outcome

Recurrence of pterygium, up to 24 months post op

24 Secondary Outcome

- Visual acuity (VA) - Intraocular pressure (IOP) - Corneal endothelial cell counts - Corneal astigmatism - Any complications from the injections

25 Study Information/Publication

i Study Information/Publication Available?

No

ii Link to Study Information/Publication

26 Last Update Date

2013-01-14

27 Primary Registry and Trial Identifying Number

ChiCTR-ONC-08000714

28 Date of Registration in Primary Registry

2010-05-04

Back History

Trial Detail