Centre For Clinical Research And Biostatistics (CCRB)

Back History

1 Unique Trial Number (assigned by CCRB)

CUHK_CCT00094

2 Trial Registration Date

2006-01-19

iRegistration Status

Retrospective

3 Secondary IDs

None

4 Source(s) of Funding

Nil

5 Primary Sponsor

Department of Paediatrics

6 Secondary Sponsor

N/A

Function

Please specify

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

i Name

Kam Lun HON

ii Address

Departmetn of Paediatrics, CUHK

iii Phone

852 26322859

iv Email

email

v Affiliation

CUHK

vi Country

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

i Name

Kam lun HON

ii Address

Departmetn of Paediatrics, CUHK

iii Phone

852 26322859

iv Email

email

v Affiliation

CUHK

vi Country

9 Official Scientific Title of the Study

A clinical trial of Tacrolimus as a therapeutic agent for atopic dermatitis in Chinese children: objective assessment of clinical efficacy in itch reduction and immunomodulatory effects

10 Public Title

A clinical trial of Tacrolimus as a therapeutic agent for atopic dermatitis in Chinese children: objective assessment of clinical efficacy in itch reduction and immunomodulatory effects

i Public Title in Chinese 研究名稱

11 Short Title (Optional)

Omit

12 Countries of Recruitment

Hong Kong, China

13Research Ethic Review

i Has the study received appropriate ethics approval?

Yes

ii When is the approval date?

2005-12-01

iii Full Name of IRB/IEC

Please specify

iv IRB/IEC approval reference number

14 Medical Condition Being Studied

Skin and Connective Tissue Diseases

15Intervention

i Types of intervention

Drug

Please specify

ii Description/ name of Intervention/article

Topical Tacrolimus

iii Dosage form of the intervention

iv Dosage of the intervention

v Duration of the intervention

2-4 weeks

vi Frequency of the intervention

16Comparative Treatments

i Description/ name of comparative treatments

placebo

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

Patients with eczema, aged 2 to 15 years

ii Exclusion Criteria

As stated before

iii Age Minimum

2

iv Age Maximum

18

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

Double-blind

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

2005-12-01

21 Target Sample Size

50+

22 Recruitment Status

Complete

23 Primary Outcome

SCORAD

24 Secondary Outcome

DigiTrac recording, chemiokines

25Study Information/Publication

i Study Information/Publication Available?

No

ii Link to Study Information/Publication

26Last Update Date

2011-04-01

27 Primary Registry and Trial Identifying Number

ChiCTR-TRC-09000738

28 Date of Registration in Primary Registry

2010-05-04

Back History

Trial Detail