Current Studies

TARGET: 200

ACROBAT: The effect of early cryoprecipitate transfusion versus standard care in women who develop severe postpartum haemorrhage: A pilot cluster randomised trial.

 

Background: 

Cryoprecipitate transfusion has been part of standard treatment for management of women who develop severe post-partum haemorrhage (PPH) in the UK for over 40 years. However, the timing when it should be introduced during the course of PPH has not been studied. Our hypothesis is that by giving cryoprecipitate earlier, we may improve fibrinogen levels and potentially stop bleeding quicker, compared to standard care where cryoprecipitate is administered later in the course of bleeding. Before proving this in a large randomised trial, we will need to test whether it is feasible to deliver different components of the trial in this feasibility study. 

Aims: 

A pilot study to assess the feasibility of early administration of cryoprecipitate, recruitment of participants and collection of outcome data, alongside a qualitative evaluation.

Study start: 1st March 2019

Study Duration: 12 Months

Recruitment Target: 200

Chief Investigator: Dr. Laura Green

https://www.isrctn.com/ISRCTN12146519

Trial Contact Details:

 

Doris Lanz

Senior Trials Manager 

Barts Research Centre for Women’s Health

Women’s Health Research Unit │ Centre for Primary Care and Public Health

Queen Mary University of London │Yvonne Carter Building │58 Turner Street │London E1 2AB

Tel: +44 (0)20 7882 5636 │ Email: d.lanz@qmul.ac.uk

Participant Information Documents:

ACROBAT Participant Information Sheet

ACROBAT Leaflet

Location

Barts Centre for Women's Health Research 
Centre for Primary Care and Public Health
Blizard Institute
Barts and The London School of Medicine and Dentistry
Yvonne Carter Building
58 Turner Street
London E1 2AB

Tel: +44 (0)20 7882 2525

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