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Evaluation of Efficacy and Safety of Intradiscal Gelified Ethanol in Refractory Cervical Discogenic Pain — DISCERV  

Discogenic Pain Clinical Trial

Official title:
Intradiscal Gelified Ethanol in Refractory Cervical Discogenic Pain : a Interventional, Prospective, Multi-center, Open-label Study.

Clinical Trial Summary

The purpose of this study is to assesse safety and efficacy of the Intradiscal Gelified Ethanol for treatment in refractory cervical discogenic pain.

Clinical Trial Description

After being informed about the study and potential tisks, all patients giving written informed consent will undergo a inclusion visit (CT scan and X ray at least) for study entry. At Day 0, operation with Intradiscal Gelified Ethanol will be performed by the investigator. Follow visit will be performed at 3 months and 12 months ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05969392
Study type Interventional
Source Gelscom SAS
Contact
Status Not yet recruiting
Phase Phase 2/Phase 3
Start date October 2023
Completion date May 2025
View Details
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