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The Cleft Registry and Audit NEtwork
Promoting excellence in cleft care
CRANE Newsletter - Issue 2018 (3) 8 October 2018 now available08/10/2018This issue includes information on: Updated CRANE consent documentation, a consultation on outcomes for children over 5 years of age, and publication of the CRANE Database 2018 Annual Report...
Summary of Findings for Patients and Parents/Carers05/07/2018Our most recent publication! In collaboration with CLAPA.
Database User Guides for Cleft Teams01/12/2017Helping Cleft Teams import data, export data, and remove duplicate cases from the Database...
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.
1073856
Records in databaseRegistrations for the 2017 birth year
Registrations for the 2018 birth year
HelpDeskNeed help - contact CRANE support on:
020 7869 6610 (Mon-Fri 9.00-5.00) E-mail: crane@rcseng.ac.uk