Actively Recruiting
Australian and New Zealand Massive Transfusion Registry
Led by Monash University · Updated on 2020-09-02
50000
Participants Needed
1
Research Sites
930 weeks
Total Duration
On this page
Sponsors
M
Monash University
Lead Sponsor
C
CSL Behring
Collaborating Sponsor
AI-Summary
What this Trial Is About
Severe and un-stopped blood loss can occur for a number of different reasons including after a serious injury, delivery of a baby and following other medical and surgical emergencies. The investigators understanding of how to best treat people with serious bleeding is still incomplete, with many questions remaining. These include questions regarding how many people have serious bleeding events, what happens to them and the best way to treat them. The Massive Transfusion Registry (MTR) is a register of patients who have experienced major blood loss that required a massive transfusion in any clinical setting. The MTR uses electronic data extraction and data linkage methodologies. Pre-existing clinical data from hospital data sources, including Laboratory Information Systems (for transfusion history and laboratory results) and Health Information Services databases (for Patient demographics and admission data), are electronically extracted by staff employed at the participating hospitals. The data is then sent to the MTR Research Team, located at Monash University, where it is then linked, analysed and stored. The establishment of a Massive Transfusion Registry will be a unique and important resource for clinicians in Australia, New Zealand and internationally, for Blood Services and for the broader community. It will provide valuable observational data regarding the types and frequency of conditions associated with critical bleeding requiring massive transfusion, the use of blood component therapy (i.e. ratios and quantities of different types of red cell to non- red cell components) and patient outcomes.
CONDITIONS
Official Title
Australian and New Zealand Massive Transfusion Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 years or over
- Received 5 or more units of red blood cells in any 4 hour period
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Monash University
Melbourne, Victoria, Australia, 3004
Actively Recruiting
Research Team
E
Erica Wood, MBBS
CONTACT
R
Rosemary Sparrow, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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