Discure Technologies Feasibility Study for DDD

Status Not yet recruiting

Clinical Trial Summary

The objective of this study is to evaluate the safety and performance of the Discure System therapy in subjects with early to moderate degeneration of the disc (DDD).

Clinical Trial Description

A prospective, interventional, multi-center, single arm, open label, feasibility study. The study is designed to evaluate the safety and performance of the Discure System in the treatment of chronic low back pain (with or without radicular pain) of discogenic origin with early to moderate degeneration of the disc (DDD) in levels L1-2 to L5-S1, as confirmed by history and radiographic studies and/or discography, who failed conservative treatment of 12 weeks in duration. Subjects will be followed at 1,3-, and 6-months post procedure. The primary endpoint will be assessed at the 6-month follow-up visit. The study will enroll up to 20 subjects at up to 8 sites. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06127745
Study type	Interventional
Source	Discure Technologies Ltd.
Contact	Shirley Giorini Silfen, PhD
Phone	+972.9.953 1125
Email	shirley@discuremd.com
Status	Not yet recruiting
Phase	N/A
Start date	January 2024
Completion date	December 2024

View Details

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