Centre For Clinical Research And Biostatistics (CCRB)

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1 Unique Trial Number (assigned by CCRB)

CUHK_CCT00105

2 Trial Registration Date

2006-02-28

i Registration Status

Prospective

3 Secondary IDs

CUHK4004-PPR20051

4 Source(s) of Funding

RGC Public Policy Research Fund

5 Primary Sponsor

Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Prince of Wales Hospital

6 Secondary Sponsor

N/A

Function

Please specify

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

i Name

Anna Lee

ii Address

Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong

iii Phone

852 2632 2735

iv Email

email: annalee@cuhk.edu.hk

v Affiliation

The Chinese University of Hong Kong

vi Country

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

i Name

Anna Lee

ii Address

Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong

iii Phone

852 2632 2735

iv Email

email: annalee@cuhk.edu.hk

v Affiliation

The Chinese University of Hong Kong

vi Country

9 Official Scientific Title of the Study

Cost-effectiveness of an anaesthesiologist-led Acute Pain Service

10 Public Title

Cost-effectiveness of an anaesthesiologist-led Acute Pain Service

i Public Title in Chinese 研究名稱

11 Short Title (Optional)

Cost-effectiveness of APS

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?

2005-07-05

iii Full Name of IRB/IEC

Please specify

iv IRB/IEC approval reference number

14 Medical Condition Being Studied

postoperative pain

15 Intervention

i Types of intervention

Other

Please specify

Acute pain management

ii Description/ name of Intervention/article

Acute Pain Service

iii Dosage form of the intervention

iv Dosage of the intervention

v Duration of the intervention

3 days

vi Frequency of the intervention

16 Comparative Treatments

i Description/ name of comparative treatments

Standard ward pain management by surgical team

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: Specific types of elective major surgery

ii Exclusion Criteria

Exclusion: childrne, mentally incompetent

iii Age Minimum

15

iv Age Maximum

100

v Gender

Both Male and Female

18 Study Type

Interventional

19 Study Design

i Randomization

Randomized

Please specify

ii Nature of control

Active

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

2006-03-06

21 Target Sample Size

560

22 Recruitment Status

Complete

23 Primary Outcome

Quality of recovery score

24 Secondary Outcome

Pain intensity, pain relief, patient satisfaction, costs

25 Study Information/Publication

i Study Information/Publication Available?

No

ii Link to Study Information/Publication

26 Last Update Date

2009-11-24

27 Primary Registry and Trial Identifying Number

28 Date of Registration in Primary Registry

* Legacy Fields

i Recruitment Information Available?

Yes

ii Link to Recruitment Information

NIL

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Trial History Detail on 2009-11-24