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NOT YET RECRUITING
NCT05969392
PHASE2/PHASE3
Evaluation of Efficacy and Safety of Intradiscal Gelified Ethanol in Refractory Cervical Discogenic Pain
Sponsor: Gelscom SAS
View on ClinicalTrials.gov
Summary
The purpose of this study is to assesse safety and efficacy of the Intradiscal Gelified Ethanol for treatment in refractory cervical discogenic pain.
Official title: Intradiscal Gelified Ethanol in Refractory Cervical Discogenic Pain : a Interventional, Prospective, Multi-center, Open-label Study.
Key Details
Gender
All
Age Range
18 Years - 120 Years
Study Type
INTERVENTIONAL
Enrollment
60
Start Date
2025-04
Completion Date
2026-04
Last Updated
2025-03-11
Healthy Volunteers
No
Conditions
Interventions
DEVICE
Intradiscal Gelified Ethanol (Discogel)
Intradiscal percutaneous injection of an intradiscal Gelified Ethanol
Locations (2)
Santissima Trinità Hospital Ascagliari
Cagliari, Italy
Azienda Ospedaliera Universitaria
Siena, Italy