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The Cleft Registry and Audit NEtwork
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Information for Patients
The 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
CRANE will report Psychology outcomes in next Annual Report
Data on Psychology outcomes at 5 years, for 2011 births, to be entered by cleft teams by June 2018.
CRANE eNewsletter - Issue 2018 (1) 12 January 2018 now available
This issue includes information on: The 2017 Annual Report - PUBLISHED AND AVAILABLE NOW. Data collection cut off dates for 2018 analyses...
Database User Guides for Cleft Teams
Helping 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, and into adulthood 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 2017 birth year
Registrations for the 2018 birth year
Need help - contact CRANE support on:
020 7869 6610 (Mon-Fri 9.00-5.00) E-mail: email@example.com