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| NB: The information displayed below does not replace the protocol. The latest protocol version should always be consulted before making clinical decisions. |
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UKAITPR
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United Kingdom Adult Idiopathic Thrombocytopenic Purpura (ITP) Registry: An Investigation of Disease Progression, Treatment Effectiveness, and Co-morbid Conditions
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Topic
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Blood
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Portfolio Eligibility
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Funded by UKCRC partner
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ISRCTN
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EudraCT
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MREC N° |
07/H0718/57
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UKCRN ID |
4961
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WHO ID
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Research Summary
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The UK Adult ITP Registry aims to collect biological samples (whole blood [15 mL, ~EDTA] or saliva [Oragene saliva kit]) and clinical data (co-morbid conditions, ITP-specific treatments, laboratory results, and bleeding events) on adult patients with primary immune thrombocytopenia (ITP) in an effort to investigate outstanding questions in disease progression, treatment effectiveness, and co-morbid burden. An overview of our study protocol may be found in the document “UKITP Study Protocol 1.6” on the Adult Registry page of our study website, www.ukitpregistry.com
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Study Type |
Observational
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Design Type |
Not specified
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Disease(s) |
Non-malignant haematology
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Phase |
N/A
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Current Status
| Open |
| Closure Date | 01/07/2017 |
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Sample Size
| 1000 |
| Accrual to Date |
 50% |
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Geographical Scope
| UK Multi-Centre |
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Lead Country
| England |
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Open to new sites
| Yes, within and outside lead country |
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Main Inclusion Criteria
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Adult patients (16 years) diagnosed with primary immune thrombocytopenia (ITP) as defined by 2002 British Committee for Standards in Haematology Guidelines
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Main Exclusion Criteria
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Not Applicable
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Chief Investigator(s)
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| Dr Drew Provan |
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Further details, please contact
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Mr Ameet Sarpatwari
Royal London Hospital
Pathology and Pharmacy Building, 80 Newark Street, London
80 Newark Street
London
E1 2ES
UNITED KINGDOM
Tel: 020 3246 0339 Ext: 61114
avs31@medschl.cam.ac.uk
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Funder(s) |
GlaxoSmithKline
ITP (Immune Thrombocytopenic Purpura) Support Association
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Sponsor(s) |
Barts and The London Trust
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