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ITP Registry and Accompanying Biospecimen Collection — ITP-Registry  

Immune Thrombocytopenia Clinical Trial

Official title:
Multicenter National ITP Registry and Accompanying Biospecimen Collection

Clinical Trial Summary

The objective of this ITP registry is to collect clinical information, including biosampling, from consenting patients with a variety of ITPs at different points in the course of their disease.

Clinical Trial Description

Immune thrombocytopenia (ITP) is a rare hematologic disorder that can lead to a greater risk of bleeding or a prolonged bleeding time due to an autoimmune-mediated deficiency of platelets. In recent years, new treatment options for patients with immune thrombocytopenia have emerged. The results of published clinical studies on ITP can only be used for broad patient care to a limited extent, as they are designed for a patient population with clearly defined inclusion and exclusion criteria. Real world data collected from this registry will help to better understand the diagnosis and therapy of ITP patients in everyday treatment and to more effectively direct individual patients to optimal therapy, thus improving their outcomes. By collecting biospecimens, this project will contribute new knowledge to the study of ITP through standardized, systematic, and high-quality collection and storage of patient samples and associated data. The registry collects clinical data from patients diagnosed with ITP at defined points in the course of the disease. The Data collection includes a range of clinical measures, disease-related factors, treatment/treatment course and outcomes, complications during treatment and Qol, fatigue scoring and survival data (up to 5 years). The data are collected prospectively. In addition, patients can be included retrospectively up to 12 months after the initial diagnosis if continuous documentation can be provided at the treatment centre. In both cases, a written declaration of consent is obligatory. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05152238
Study type Observational [Patient Registry]
Source Jena University Hospital
Contact Thomas Stauch, Dr. med.
Phone 0049-3641-9326864
Email thomas.stauch@med.uni-jena.de
Status Recruiting
Phase
Start date November 29, 2021
Completion date April 2027
View Details
See also
  Status Clinical Trial Phase
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