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Open-Label Placebo for Non-Specific Pain in the ED — OLP_EM  

Pain, Acute Clinical Trial

Official title:
Open -Label Placebo for Non-specific Pain in the Emergency Department: Study Protocol for a Mixed-method Randomised Control Feasibility Study

Clinical Trial Summary

The aim of this study is to assess whether an intervention with open-label placebo (OLP) for non-specific pain in the emergency department is feasible.

Clinical Trial Description

This project is a collaboration between the Emergency Department at the University Hospital of Basel and the Faculty of Psychology at the University of Basel. The investigation will analyze whether an intervention consisting of open-label placebo tablets is feasible for patients with non-specific pain in the emergency department. Open-label placebos are administered without deception, meaning the patients are aware they are taking a placebo. Patients will be randomized into intervention group (OLP) or control group (treatment as usual) with ibuprofen. The study duration for patients is 30 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06408519
Study type Interventional
Source University Hospital, Basel, Switzerland
Contact Bruno Minotti, MD
Phone +41615565324
Email bruno.minotti@usb.ch
Status Recruiting
Phase N/A
Start date May 23, 2024
Completion date May 2025
View Details
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