Centre For Clinical Research And Biostatistics (CCRB)

Back History

1 Unique Trial Number (assigned by CCRB)

CUHK_CCT00144

2 Trial Registration Date

2007-09-11

iRegistration Status

Prospective

3 Secondary IDs

nil

4 Source(s) of Funding

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

5 Primary Sponsor

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

6 Secondary Sponsor

n/a

Function

Please specify

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

i Name

Professor Warwick D. Ngan Kee

ii Address

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

iii Phone

+852 26322735

iv Email

warwick@cuhk.edu.hk

v Affiliation

The Chinese University of Hong Kong

vi Country

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

i Name

Professor Warwick D. Ngan Kee

ii Address

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

iii Phone

+852 26322735

iv Email

warwick@cuhk.edu.hk

v Affiliation

The Chinese University of Hong Kong

vi Country

9 Official Scientific Title of the Study

Randomized comparison of computer-controlled versus manual infusion of phenylephrine for maintaining maternal blood pressure during spinal anaesthesia for Caesarean section

10 Public Title

Randomized comparison of computer-controlled versus manual infusion of phenylephrine for maintaining maternal blood pressure during spinal anaesthesia for Caesarean section

i Public Title in Chinese 研究名稱

11 Short Title (Optional)

Computer controlled vasopressors in obstetric anaesthesia

12 Countries of Recruitment

Hong Kong

13Research Ethic Review

i Has the study received appropriate ethics approval?

Yes

ii When is the approval date?

2007-09-04

iii Full Name of IRB/IEC

Please specify

iv IRB/IEC approval reference number

14 Medical Condition Being Studied

Pregnancy/Caesarean section

15Intervention

i Types of intervention

Procedure

Please specify

ii Description/ name of Intervention/article

Computer-controlled closed-loop feedback phenylephrine infusion

iii Dosage form of the intervention

iv Dosage of the intervention

v Duration of the intervention

approx 30 min

vi Frequency of the intervention

16Comparative Treatments

i Description/ name of comparative treatments

1. Computer-controlled closed-loop feedback phenylephrine infusion 2. Manual-controlled phenylephrine infusion

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: Healthy, term, singleton parturients having elective Caesarean section under spinal anaesthesia.

ii Exclusion Criteria

Exclusion criteria: Onset of labour, hypertension, cardiac disease, cerebrovascular disease, fetal abnormality

iii Age Minimum

18

iv Age Maximum

50

v Gender

Female

18 Study Type

Interventional

19Study 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

2007-11-01

21 Target Sample Size

222

22 Recruitment Status

Complete

23 Primary Outcome

Median absolute performance error of serial systolic blood pressure versus baseline

24 Secondary Outcome

n/a

25Study Information/Publication

i Study Information/Publication Available?

No

ii Link to Study Information/Publication

26Last Update Date

2013-01-10

27 Primary Registry and Trial Identifying Number

ChiCTR-TRC-09000702

28 Date of Registration in Primary Registry

2010-05-04

Back History

Trial Detail