We'd like your feedback
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Claudia
Grimaldo
csor@npeu.ox.ac.uk
Claudia
Grimaldo
csor@npeu.ox.ac.uk
Prof
Marian
Knight
marian.knight@npeu.ox.ac.uk
More information about this study, what is involved and how to take part can be found on the study website.
Digestive system disorders of fetus and newbornCongenital malformations and deformations of the musculoskeletal systemCongenital malformations of the urinary systemOther congenital malformations of the digestive system
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
There is currently significant variation between hospitals in the way children with a range of surgical conditions are treated. Examples of variation include the age or weight at which a planned operation is carried out,the type of operation a child gets,and how quickly they are allowed to start feeding after an operation. It is not currently known which elements of variation in management affect how successfully a child is treated. The aim of the Children’s Surgery Outcome Reporting (CSOR) Research Database is to combine three sources of information about children with surgical conditions in order to understand more about how different hospitals treat children with surgical conditions,and how successfully children in these hospitals are treated. This information will be used to help understand which elements of variation in management affect how successfully children are treated. The information will also be used to help hospitals understand how they can treat children with surgical conditions more successfully,and to answer important questions that could improve the health and wellbeing of children with surgical conditions. Some of the information that is used in the CSOR research database will be collected directly from children’s electronic patient records,some will be collected from routine national sources of data,and some will be collected directly from children’s parents. To begin with,the CSOR research database will collect information about children with necrotising enterocolitis,Hirschsprung’s disease,gastroschisis,congenital diaphragmatic hernia,oesophageal atresia and posterior urethral valves. However,it is expected that in the future,the database will also collect information about children with other surgical conditions.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
Observational type: Cohort study;
You can take part if:
You may not be able to take part if:
None
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Prof
Marian
Knight
marian.knight@npeu.ox.ac.uk
Claudia
Grimaldo
csor@npeu.ox.ac.uk
Claudia
Grimaldo
csor@npeu.ox.ac.uk
More information about this study, what is involved and how to take part can be found on the study website.
The study is sponsored by University of Oxford and funded by NIHR Evaluation, Trials and Studies Co-ordinating Centre (NETSCC) .
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Read full details
for Trial ID: CPMS 55462
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
