Norwegian Acute Pain Service (APS) Registry

The Norwegian APS registry collects data from hospitalized patients referred to the APS during their hospital stay. These patients normally have difficult pain conditions that don’t respond to standard ward pain care. Patients that fulfill a set of inclusion criteria and give a written consent are included in the registry.

Criteria for data access

The data sources have different purposes and are regulated by different laws and regulations. In order to access information from the data sources, what you plan to use the information for must be in accordance with the purpose of the data source.

The types of approvals and documents you must submit to access information depend on what you are applying for, what you are going to use the information for and how you are going to process it. We therefore recommend that you take the time to familiarize yourself with the application guides before starting the application process:

Application guide for anonymous, aggregated data (statistical data)
Application guide for personally identifiable data

Apply for access to data

Contact the data custodian for more information on how to access data from the registry.

Contact

Lars Jørgen Rygh, overlege

Links