Building a Swiss Pain Registry: A National Framework for Acute and Chronic Pain Assessment

Starting soon

Conditions studied: Chronic Pain, Acute Pain

In brief

The goal of this observational registry is to systematically collect and analyse real-world clinical and patient-reported data in individuals receiving treatment for acute and chronic pain. The main questions it aims to answer are: How do pain intensity, functional status, and quality of life evolve over time in patients with acute and chronic pain? How are different routine clinical treatment approaches associated with patient-reported outcomes in real-world clinical practice? Participants already receiving standard care for pain management will have routine clinical data recorded as part of their treatment and will be asked to complete standardized questionnaires on pain intensity, functional status, and quality of life at multiple time points during treatment and follow-up. Data are collected using a secure electronic system and are pseudonymised prior to analysis in accordance with Swiss data protection regulations.

Key facts

Study ID
NCT07717762
Run by
Insel Gruppe AG, University Hospital Bern
People needed
500
Starts
2026-07-15
Expected to finish
2029-08-15
Last updated by the study team
2026-07-21

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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