Registering a new trial?

To achieve prospective registration, we recommend submitting your trial for registration at the same time as ethics submission.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial registered on ANZCTR


Registration number
ACTRN12606000038594
Ethics application status
Approved
Date submitted
25/11/2005
Date registered
25/01/2006
Date last updated
25/01/2006
Type of registration
Retrospectively registered

Titles & IDs
Public title
Use of transthoracic echocardiography to assess left ventricular volume in total hip joint replacement.
Scientific title
Use of transthoracic echocardiography to assess left ventricular volume in total hip joint replacement.
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Left ventricular volume assessment. 1000 0
Condition category
Condition code
Cardiovascular 1075 1075 0 0
Normal development and function of the cardiovascular system
Musculoskeletal 1076 1076 0 0
Other surgery

Intervention/exposure
Study type
Observational
Patient registry
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
The aim of this project is to assess the abiltiy of the anaesthetist to estimate volume status of the patient utilising traditional clinical methods, when compared to measurements obtained by transthoracic echocardiography. A transthoracic echocardiogram (TTE) is done at baseline (before the spinal anaestheisa is performed), immediately after spinal anesthesia is performed and after the hip replacement surgery is complete.
Intervention code [1] 772 0
None
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 1441 0
Assessing the anaesthetists ability to estimate volume status of the patient when utilising traditional clinical methods
Timepoint [1] 1441 0
Immediately post spinal anaesthesia and immediately post op
Secondary outcome [1] 2551 0
There are no secondary outcomes.
Timepoint [1] 2551 0

Eligibility
Key inclusion criteria
Patients undergoing elective right sided total hip joint replacement.
Minimum age
Not stated
Maximum age
Not stated
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Patients with contraindications to spinal anaesthesia. Poorly compensated cardiac failure.

Study design
Purpose
Screening
Duration
Cross-sectional
Selection
Convenience sample
Timing
Prospective
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)

Funding & Sponsors
Funding source category [1] 1178 0
Government body
Name [1] 1178 0
NHMRC grant
Country [1] 1178 0
Australia
Primary sponsor type
Hospital
Name
Department of Anaesthesia, St Vincent's Hospital, Melbourne
Address
Country
Australia
Secondary sponsor category [1] 1038 0
None
Name [1] 1038 0
Nil
Address [1] 1038 0
Country [1] 1038 0

Ethics approval
Ethics application status
Approved

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 35495 0
Address 35495 0
Country 35495 0
Phone 35495 0
Fax 35495 0
Email 35495 0
Contact person for public queries
Name 9961 0
Ms Simone Said
Address 9961 0
Department of Anaesthesia
St Vincent's Hospital Melbourne
PO Box 2900
Fitzroy VIC 3065
Country 9961 0
Australia
Phone 9961 0
+61 3 92884245
Fax 9961 0
Email 9961 0
Contact person for scientific queries
Name 889 0
Dr Christopher Hoy
Address 889 0
Department of Anaesthesia
St Vincent's Hospital Melbourne
PO Box 2900
Fitzroy VIC 3065
Country 889 0
Australia
Phone 889 0
+61 3 92884245
Fax 889 0
Email 889 0

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.