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Trial registered on ANZCTR
Registration number
ACTRN12613001043729
Ethics application status
Submitted, not yet approved
Date submitted
16/09/2013
Date registered
19/09/2013
Date last updated
15/10/2015
Type of registration
Prospectively registered
Titles & IDs
Public title
Novel use of tranexamic acid in major joint surgery
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Scientific title
Prospective randomised equivalence trial to compare blood loss and transfusion rates for periarticular and intravenous administration of tranexamic acid in primary hip and knee joint arthroplasty.
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Secondary ID [1]
283223
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Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Anaemia
290096
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Major Joint Surgery
290106
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Condition category
Condition code
Blood
290470
290470
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0
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Anaemia
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Surgery
290485
290485
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0
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Other surgery
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
1 gram of tranexamic acid directly infiltrated into the periarticular tissues mixed with the standard local anaesthetic solution. The local infiltration analgesic (LIA) mixture consists of 150mls of 0.2% ropivicaine with 5micrograms per ml of adrenaline.
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Intervention code [1]
287953
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Treatment: Drugs
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Comparator / control treatment
1 gram of tranexamic acid given intravenously during surgery followed by another 1 gram six hours post-operatively.
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Control group
Active
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Outcomes
Primary outcome [1]
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Blood loss as calculated by the haemoglobin balance method.
This method assumes that the blood volume (BV in ml) on the 5fth day after surgery is the same as that before surgery. BV is estimated by taking sex, body mass and height into account. The loss of Hb (in grams) was then estimated according to the formula:
Hb loss=BV x (Hbi-Hbe) x 0.001+Hbt
where Hb loss (g) is the amount of Hb lost, Hbi (g/litre) the
Hb concentration before surgery, Hbe (g/litre) is the Hb
concentration on the 5fth day after surgery and Hbt (g) is the
total amount of allogeneic Hb transfused. A unit of banked
blood was considered to contain 63g Hb at our institution. The blood loss (ml) was related to the patient's preoperative Hb value (g/litre):
Blood loss =1000 x Hbloss/Hbi
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Assessment method [1]
290495
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Timepoint [1]
290495
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Preoperative Hb and Postoperative Day 1,3, & 5.
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Secondary outcome [1]
304633
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Red Cell Transfusion rates. The number of units of red cell transfusion administered during the post-operative in-patient stay will be recorded.
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Assessment method [1]
304633
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Timepoint [1]
304633
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red cell transfusion rates will be recorded at any time during the inaptient stay up to 1 week post-operatively.
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Eligibility
Key inclusion criteria
Primary unilateral total hip arthroplasty
Primary unilateral total knee arthroplasty
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Revision Hip or Knee Arthroplasty
Unicompartment (Oxford) knee arthroplasty
Cardiac Stents
Prior stroke or myocardial infarction
History of deep venous thrombosis or pulmonary embolus
Any thrombophilia
Oral contraceptive pill
Pregnancy or breast feeding
End stage renal failure
Peripheral vascular disease with vascular stents
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
All patients referred for joint replacement surgery to the nominated surgeons consecutively.
Allocation concealment by concealed envelopes.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
A web based randomization schedule will be used to randomize
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
Equivalence trial
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Phase
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
An equivalence test of means using two one-sided tests on data from a parallel-group design with sample sizes of 45 in the reference group and 45 in the treatment group achieves 81% power at a 5% significance level when the true difference between the means is 0, the standard deviation is 480mls, and the equivalence limits are -300mls and 300mls.
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Recruitment
Recruitment status
Withdrawn
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Reason for early stopping/withdrawal
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Date of first participant enrolment
Anticipated
1/06/2014
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Actual
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Date of last participant enrolment
Anticipated
5/01/2015
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
100
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
1524
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Hollywood Private Hospital - Nedlands
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Recruitment postcode(s) [1]
7362
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6009 - Nedlands
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Funding & Sponsors
Funding source category [1]
287972
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Self funded/Unfunded
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Name [1]
287972
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Address [1]
287972
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Country [1]
287972
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Primary sponsor type
Individual
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Name
Dr Mark J Lennon
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Address
Hollywood Private Hospital
Monash Avenue
Nedlands
WA 6009
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Country
Australia
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Secondary sponsor category [1]
286692
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Individual
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Name [1]
286692
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Professor Riaz Khan
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Address [1]
286692
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The Joint Studio
Suite 1 Hollywood Medical Centre
85 Monash Avenue, Nedlands 6009
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Country [1]
286692
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Australia
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Ethics approval
Ethics application status
Submitted, not yet approved
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Ethics committee name [1]
289897
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Hollywood Hospital Research Ethics Committee
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Ethics committee address [1]
289897
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Hollywood Private Hospital Locked Bag 2002 NEDLANDS, WA 6909
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Ethics committee country [1]
289897
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Australia
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Date submitted for ethics approval [1]
289897
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16/09/2013
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Approval date [1]
289897
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Ethics approval number [1]
289897
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Summary
Brief summary
Major joint surgery is associated with significant blood loss which often requires transfusion. Tranexamic acid is a recommended medication to assist with limiting blood loss. It acts by preventing the breakdown of blood clot. The usual dosage is multiple intravenous injections. The optimal dose is unknown. This study will examine the effects of direct injection of tranexamic acid into the site of surgery and compare this to the intravenous route. The hypothesis is that this will be as effective if not more effective than intravenous use and is easier to administer.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
42978
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Dr Mark J Lennon
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Address
42978
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Hollywood Private Hospital
Monash Avenue
Nedlands
WA 6009
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Country
42978
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Australia
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Phone
42978
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+61 8 93466000
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Fax
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Email
42978
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[email protected]
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Contact person for public queries
Name
42979
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Mark J Lennon
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Address
42979
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Hollywood Private Hospital
Monash Avenue
Nedlands
WA 6009
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Country
42979
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Australia
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Phone
42979
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+61 8 93466000
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Fax
42979
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Email
42979
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[email protected]
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Contact person for scientific queries
Name
42980
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Mark J Lennon
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Address
42980
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Hollywood Private Hospital
Monash Avenue
Nedlands
WA 6009
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Country
42980
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Australia
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Phone
42980
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+61 8 93466000
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Fax
42980
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Email
42980
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[email protected]
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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.
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