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Vonicog Alfa (Recombinant Von Willebrand Factor) Treatment Outcomes in Von Willebrand Disease in the UK: a Retrospective Chart Review Study
This study is a retrospective chart review study and will collect data on real world use of vonicog alfa (Recombinant Von Willebrand Factor \[rVWF\]). Von Willebrand disease (VWD) is the most common inherited bleeding disorder. rVWF is approved in Europe and UK to treat bleeding and to treat and prevent bleeding during surgeries in adults in 2018. This study will review and collect information on the treatment and bleed prevention of adult persons with inherited VWD with rVWF in UK. These data were already collected as a part of the routine care. The main aims of this study are to describe the use of rVWF in on-demand treatment of bleeding and the prevention of treatment and treatment of bleeding during surgeries. Other aims are to describe bleedings and their treatment as well as any surgeries before and after first treatment with rVWF and to gather information on the use of healthcare resources (such as hospital visits, emergency room visits, etc.).
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
University Hospitals Birmingham
Birmingham, United Kingdom
Leeds Teaching Hospital
Leeds, United Kingdom
Liverpool University Hospital
Liverpool, United Kingdom
Royal Free London
London, United Kingdom
Imperial College Healthcare
London, United Kingdom
Manchester University
Manchester, United Kingdom
Oxford University Hospital
Oxford, United Kingdom
Start Date
December 16, 2021
Primary Completion Date
October 30, 2023
Completion Date
October 30, 2023
Last Updated
March 11, 2026
34
ACTUAL participants
No Intervention
OTHER
Lead Sponsor
Takeda
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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