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Clinical Trial Summary

Refractory pain is a prevalent condition that negatively affects patients' quality of life. Intrathecal implantable systems have been proposed as a treatment option for refractory pain. However, real-world data on the effectiveness and safety of these therapies in Spain are scarce. This study aims to obtain real-world data on the effectiveness and safety of intrathecal implantable systems for refractory pain treatment in Spain.


Clinical Trial Description

All Spanish hospitals that implant intrathecal systems for refractory pain will be invited to participate in the study. Patients will be recruited before the procedure, and before providing data to the registry, the study will be explained to them, and they will sign an informed consent form. Demographic data related to the pathology and procedure will be collected. Follow-up will be conducted at three and twelve months after the procedure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05970081
Study type Observational [Patient Registry]
Source Sociedad Espanola del Dolor
Contact Antonio Ojeda, MD
Phone 0034911729144
Email renased@sedolor.es
Status Recruiting
Phase
Start date August 1, 2023
Completion date August 1, 2025

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