A registry for ITP and other platelet disorders
ITP Natural History Study Registry
Enroll now in PDSA’s National Patient Registry dedicated to those who have a platelet disorder such as ITP to advance research and improve the quality of life for patients and their caregivers.
For more information, contact PDSA, 1.87.PLATELET (877.528.3538) or email, research@pdsa.org.
For more information about how to register, click here.
For Patients
Get Involved
Information collected during this study may be used to help provide opportunities for patients and researchers to collaborate in the rare disease community.
For Researchers
Drive Research
This is a unique rare disease patient registry. Are you interested in using our data to further your rare disease research?