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The Cleft Registry and Audit NEtwork
Promoting excellence in cleft care
@CRANE News 01/10/2019Follow us on Twitter!
User Guides for Cleft Teams30/07/2019 Guides to help Cleft Teams: 1. Manage patient records - including transfers from/to other cleft centres 2. Check data
The Cleft Registry and Audit NEtwork (CRANE) Database collects information about all children born with cleft lip and/or cleft palate in England, Wales and Northern Ireland. This database was set up by the Department of Health in 2000.

Typically, children with a cleft lip and/or palate need a mixture of care, from birth to adulthood, from professionals from different disciplines. This is why it is important to record information on these children from birth or diagnosis, to inform their care.

The database is funded by the National Health Service through the Specialist Service Commissioners, who have responsibility for the delivery of care to children born with cleft lip and palate in England, Wales, and Northern Ireland. An independent body, the Cleft Development Board, which represents patient representative groups, clinicians and commissioners, has the overall responsibility for running the database.


Copyright © CRANE 2016
High security levelThis database is fully secure and meets all data protection and information governance requirements.
1009687
Records in databaseRegistrations for the 2018 birth year
Registrations for the 2019 birth year
HelpDeskNeed help - contact CRANE support on:
020 7869 6610 (Mon-Fri 9.00-5.00) E-mail: crane@rcseng.ac.uk