Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12616000723482
Ethics application status
Approved
Date submitted
27/05/2016
Date registered
1/06/2016
Date last updated
28/11/2018
Date data sharing statement initially provided
28/11/2018
Date results provided
28/11/2018
Type of registration
Prospectively registered

Titles & IDs
Public title
Intravenous tranexamic acid ("TXA") and its effect on operating conditions, blood loss, post-operative pain and complications in patients undergoing total shoulder replacement.
Scientific title
Effect of systemic tranexamic acid use on operating conditions, blood loss, post-operative pain and complications in patients undergoing shoulder arthroplasty.
Secondary ID [1] 289324 0
None
Universal Trial Number (UTN)
U1111-1183-3447
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Blood loss in total shoulder arthroplasty 298920 0
Condition category
Condition code
Musculoskeletal 298998 298998 0 0
Osteoarthritis
Surgery 298999 298999 0 0
Other surgery

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Group 1 (TXA group) will receive 2000mg (20ml) of Tranexamic Acid (TXA) intravenously 5 minutes before incision.
Intervention code [1] 294880 0
Treatment: Drugs
Comparator / control treatment
Group 2 (Control group) will receive 2000mg (20ml) of Saline intravenously 5 minutes before incision..
Control group
Placebo

Outcomes
Primary outcome [1] 298471 0
Change in haemaglobin level as measured by the difference between pre-operative and post-operative levels as assessed by serum assay.
Timepoint [1] 298471 0
Pre-operative haemaglobin will be assessed the day before operation. Post-operative haemaglobin will be assessed in the morning of the first day after operation.
Primary outcome [2] 298485 0
Change in haemocrit as measured by the difference between pre-operative and post-operative levels as assessed by serum assay.
Timepoint [2] 298485 0
Pre-operative haemocrit will be assessed the day before operation. Post-operative haemocrit will be assessed in the morning of the first day after operation.
Secondary outcome [1] 324233 0
Operative time defined as time from induction of anaesthesia until wound closure as timed by surgical assistant with stopwatch.
Timepoint [1] 324233 0
Operative time will be calculated at the conclusion of the operation (day 0).
Secondary outcome [2] 324234 0
Transfusion requirement as measured by data linkage to patient medical records.
Timepoint [2] 324234 0
Within 6 weeks after intervention commencement.
Secondary outcome [3] 324235 0
Pain assessment using visual analogue score.
Timepoint [3] 324235 0
Measured daily for 5 days starting from 24 hours after operation.
Secondary outcome [4] 324236 0
Passive shoulder range of motion by using a goniometer.
Timepoint [4] 324236 0
Day 3, 2 weeks and 8 weeks post operation.
Secondary outcome [5] 324237 0
Infection rates as measured by data linkage to patient medical records.
Timepoint [5] 324237 0
Within 6 weeks after intervention commencement.
Secondary outcome [6] 324238 0
Thromboembolic adverse events as measured by data linkage to patient medical records.
Timepoint [6] 324238 0
Within 6 weeks after intervention commencement.
Secondary outcome [7] 324294 0
Procedure complexity rating as measured by the operating surgeon selecting either "more complex than usual", "as usual" or "less complex than usual" on a checklist.
Timepoint [7] 324294 0
At the conclusion of the operation.
Secondary outcome [8] 324295 0
Operative field visibility rating as measured by the operating surgeon selecting either "excellent", "good", "fair"or "poor" on a checklist.
Timepoint [8] 324295 0
At the conclusion of the operation.
Secondary outcome [9] 324296 0
Drain output measured in cc.
Timepoint [9] 324296 0
8 hours post operation, 16 hours post operation and 24 hours post operation.
Secondary outcome [10] 324297 0
Post-operative haematoma occurrence as measured by data linkage to patient medical records.
Timepoint [10] 324297 0
Within 24 hours post operation.
Secondary outcome [11] 324298 0
Time spent in recovery room as measured by the difference between time of arrival to time of departure.
Timepoint [11] 324298 0
Time of departure from recovery room.
Secondary outcome [12] 324299 0
Time spent in hospital as measured by the difference between date of admission to date of discharge.
Timepoint [12] 324299 0
Date of discharge.

Eligibility
Key inclusion criteria
1. Patients who have consented for anatomic or reverse shoulder arthroplasty under one of the principal investigators.
2. Patients who are capable of and have given informed consent for their participation in this study.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Patients allergic to tranexamic acid
2. Patients with a failed arthroplasty requiring revision
3. Patients with history of deep venous thrombosis or pulmonary embolism
4. Patients with cardiovascular disease, including coronary disease or peripheral arteriopathy
5. Patients with renal or liver failure
6. Patients with a known coagulopathy
7. Patients that refuse a potential transfusion

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Central randomisation by computer.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a randomisation table created by computer software (i.e. computerised sequence generation).
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s

The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
None.
Phase
Phase 4
Type of endpoint/s
Efficacy
Statistical methods / analysis
Sample size was calculated based on the primary objective. It was decided to replicate work done by Gillespie et al (2015) who found an average change in haemaglobin level of 2.6g/dL in the placebo group and 1.7g/dL in the TXA group (p < .001) with 111 patients. It was decided that increasing the subjects from 111 to 150 patients might improve the power of the study.

Correlation analysis, including univariate and multivariate analyses will be used to determine the correlation between systemic administration of TXA and the selected outcome criteria. Subgroup analysis will be carried between the different types of prosthesis (reverse versus anatomic). P value <0.5 will be considered as statistically significant. All data will be entered into Socrates Orthopaedic Outcomes Software (Ortholink Pty Ltd, Sydney, Australia).

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
31/10/2016
Actual
17/10/2016
Date of last participant enrolment
Anticipated
28/04/2017
Actual
25/08/2017
Date of last data collection
Anticipated
Actual
19/10/2017
Sample size
Target
150
Accrual to date
Final
60
Recruitment in Australia
Recruitment state(s)
NSW
Recruitment hospital [1] 5861 0
North Shore Private Hospital - St Leonards
Recruitment hospital [2] 5862 0
Mater Sydney - North Sydney
Recruitment hospital [3] 6783 0
Royal North Shore Hospital - St Leonards
Recruitment postcode(s) [1] 13302 0
2065 - St Leonards
Recruitment postcode(s) [2] 13309 0
2060 - North Sydney
Recruitment postcode(s) [3] 14439 0
2065 - Royal North Shore Hospital

Funding & Sponsors
Funding source category [1] 293697 0
Other Collaborative groups
Name [1] 293697 0
Sydney Shoulder Research Institute
Country [1] 293697 0
Australia
Primary sponsor type
Individual
Name
Dr Benjamin Cass
Address
Sydney Shoulder Research Institute
Suite 201
Level 2
156 Pacific Highway
St Leonards NSW 2065
Country
Australia
Secondary sponsor category [1] 292531 0
None
Name [1] 292531 0
Address [1] 292531 0
Country [1] 292531 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 295137 0
North Shore Private Hospital Ethics Committee
Ethics committee address [1] 295137 0
Ethics committee country [1] 295137 0
Australia
Date submitted for ethics approval [1] 295137 0
11/04/2016
Approval date [1] 295137 0
25/10/2016
Ethics approval number [1] 295137 0
Ethics committee name [2] 295138 0
St Vincent's Hospital Sydney Human Research Ethics Committee
Ethics committee address [2] 295138 0
Ethics committee country [2] 295138 0
Australia
Date submitted for ethics approval [2] 295138 0
11/05/2016
Approval date [2] 295138 0
13/09/2016
Ethics approval number [2] 295138 0

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

Contacts
Principal investigator
Name 66246 0
Dr Benjamin Cass
Address 66246 0
Sydney Shoulder Research Institute
Suite 201, Level 2
156 Pacific Highway
St Leonards NSW 2065
Country 66246 0
Australia
Phone 66246 0
+61 2 9460 8888
Fax 66246 0
+61 2 9460 6064
Email 66246 0
[email protected]
Contact person for public queries
Name 66247 0
Jasmin Gwynne
Address 66247 0
Sydney Shoulder Research Institute
Suite 201, Level 2
156 Pacific Highway
St Leonards NSW 2065
Country 66247 0
Australia
Phone 66247 0
+61 2 9460 8813
Fax 66247 0
+61 2 9460 6064
Email 66247 0
[email protected]
Contact person for scientific queries
Name 66248 0
Benjamin Cass
Address 66248 0
Sydney Shoulder Research Institute
Suite 201, Level 2
156 Pacific Highway
St Leonards NSW 2065
Country 66248 0
Australia
Phone 66248 0
+61 2 9460 8888
Fax 66248 0
+61 2 9460 6064
Email 66248 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
Now that analysis has been completed, all study data has been deidentified, stored confidentially and will not be used for any further research unless further ethics approval is granted.



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
SourceTitleYear of PublicationDOI
EmbaseA single dose of tranexamic acid reduces blood loss after reverse and anatomic shoulder arthroplasty: a randomized controlled trial.2021https://dx.doi.org/10.1016/j.jse.2020.11.022
N.B. These documents automatically identified may not have been verified by the study sponsor.