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The Cleft Registry and Audit NEtwork
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Information for Patients
Cleft Development Group
Tables & Charts
Table 1. Births by region
Table 2. Births by cleft type
Table 3. Diagnosis time
Promoting excellence in cleft care
Download August 2019 CRANE Newsletter
Issue 2019 (2) 6 August 2019 - now available!
Scott's radio interview about cleft
Our CRANE Clinical Lead talked about cleft and CRANE on Somerset BBC Radio. Tune in at 1hr & 10mins! Available online until 20 August 2019.
User Guides for Cleft Teams
Guides to help Cleft Teams: 1. Manage patient records - including transfers from/to other cleft centres 2. Check data
Data Collection Milestones for 2019/20
Please check data submission deadlines for CRANE 2020 reports
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 level
This database is fully secure and meets all data protection and information governance requirements.
Records in database
Registrations for the 2018 birth year
Registrations for the 2019 birth year
Need help - contact CRANE support on:
020 7869 6610 (Mon-Fri 9.00-5.00) E-mail: email@example.com