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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

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