Vitaccess Real CIDP Registry

Launched by VITACCESS LTD · Jun 4, 2025

Keywords

ClinConnect Summary

The Vitaccess Real CIDP Registry is a long-term study designed to better understand Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), a condition that affects the nerves and can lead to weakness and other symptoms. Over the next 10 years, this registry will collect information from around 300 patients in the US and Europe about their experiences with CIDP, including how it affects their daily lives and the treatments they receive. Participants will share their own health information, which will be linked to their medical records to create a comprehensive view of CIDP.

To join the study, participants must be at least 18 years old, have a confirmed diagnosis of CIDP from a neurologist, and live in the US, UK, or Germany. They also need to have access to a smartphone, tablet, or computer and be willing to provide consent in their preferred language. The study is not currently recruiting, but when it begins, participants can expect to share their experiences, which will help improve understanding and treatment of CIDP for everyone affected by this condition.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Adult (age ≥18 years) with a clinically confirmed diagnosis of CIDP by their treating neurologist
• • Resident in the US, UK or Germany
• • Access to a smartphone/tablet/computer/laptop
• • Willing and able to provide informed consent in their local language to take part in the study
• Exclusion Criteria:
• • None