Welcome to the
UK-ITP Paediatric Registry
Support Site
Support Site
The UK Paediatric ITP registry is a multi-centre study designed to collect prospective data on all new cases of childhood immune thrombocytopenic purpura (ITP). Recruitment is open to all patients between the ages of 2 months and 18 years that have been diagnosed at any time.
The database will continue to collect data for many years about children whose ITP fails to resolve. Clinical data, bleeding severity, platelet counts and management will be recorded.
The Registry is generously supported by the ITP Support Association
From the 1st March 2024 the ITP Study is now closed.
If you require IT assistance, please email the MDSAS IT support team support@mdsas.com, or call on 0161 850 5075.