Centre For Clinical Research And Biostatistics (CCRB)

Back History

1 Unique Trial Number (assigned by CCRB)

CUHK_CCT00060

2 Trial Registration Date

2005-09-09

iRegistration Status

Retrospective

3 Secondary IDs

n/a

4 Source(s) of Funding

RGC Grant

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

Benny Fok

ii Address

Department of Medicine and Therapeutics

iii Phone

26323377

iv Email

bfok@cuhk.edu.hk

v Affiliation

The Chinese University of Hong Kong

vi Country

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

i Name

Kenneth KC Lee

ii Address

School of Pharmacy

iii Phone

26096827

iv Email

kclee@cuhk.edu.hk

v Affiliation

The Chinese University of Hong Kong

vi Country

9 Official Scientific Title of the Study

The effect of Orlistat and Rosiglitazone on insulin action in a grouop of Chinese patients affected by the metabolic syndrome -- a randomized, single-blinded and placebo controlled study

10 Public Title

The effect of Orlistat and Rosiglitazone on insulin action in a grouop of Chinese patients affected by the metabolic syndrome -- a randomized, single-blinded and placebo controlled study

i Public Title in Chinese 研究名稱

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?

1999-09-08

iii Full Name of IRB/IEC

Please specify

iv IRB/IEC approval reference number

14 Medical Condition Being Studied

Gland and Hormone Related Diseases

15Intervention

i Types of intervention

Drug

Please specify

ii Description/ name of Intervention/article

Orlistat

iii Dosage form of the intervention

iv Dosage of the intervention

v Duration of the intervention

1 year

vi Frequency of the intervention

16Comparative Treatments

i Description/ name of comparative treatments

Rosiglitazone

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 impaired glucose tolerance or type 2 diabetes

ii Exclusion Criteria

Patients on insulin or requiring more than one diabetic medication

iii Age Minimum

18

iv Age Maximum

75

v Gender

Both Male and Female

18 Study Type

Interventional

19Study Design

i Randomization

Randomized

Please specify

ii Nature of control

Active

iii Degree of masking

Single-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

2001-07-01

21 Target Sample Size

75

22 Recruitment Status

Complete

23 Primary Outcome

insulin action in patients with impaired glucose tolerance or type 2 diabetes

24 Secondary Outcome

changes in cardiovascular risk factors

25Study Information/Publication

i Study Information/Publication Available?

No

ii Link to Study Information/Publication

26Last Update Date

2009-11-27

27 Primary Registry and Trial Identifying Number

ChiCTR-TRC-09000652

28 Date of Registration in Primary Registry

2010-05-04

Back History

Trial Detail