Information for Researchers

The Arachnoiditis Patient Registry collects disease-specific natural history data about individuals with Arachnoiditis, with the goal of improving the understanding of Arachnoiditis and informing treatment development. Registry questionnaires were built from common data element standards and cover the following topics:

If you would like access to the Arachnoiditis Patient Registry data for a research project, please contact our registry administrator at nordregistry@rarediseases.org. Access to Arachnoiditis Patient Registry data is contingent upon project approval by the NORD Registry Advisory Board.