ITP Registry and Accompanying Biospecimen Collection
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- Jena University Hospital
- Trial code
- NCT05152238
- Record updated
- 15 July 2025
- Original description
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.Read full original descriptionShow less
Multicenter National ITP Registry and Accompanying Biospecimen Collection
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.
Inclusion: Primary or secondary Immune Thrombocytopenia (ITP); Age ≥18 years; signed declaration of consent.
Exclusion: diagnoses that cannot be reconciled with the diagnosis of ITP (esp. heparin-induced thrombocytopenia, pregnancy-associated thrombocytopenia, pseudothrombocytopenia); no informed consent possible (this covers patients who are unable to understand the nature and scope of participation).