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Post-marketing Clinical Follow-up of the Medical Device DIVA®

Lumbar Disc Herniation Clinical Trial

Official title:
Clinical Follow-up of the DIVA® Device in Lumbar Disc Herniation Surgery

Clinical Trial Summary

Observational, ambispective, longitudinal, comparative, open, multicentric study. The main objective is to compare the performance of care in patients operated with and without DIVA®.

Clinical Trial Description

The primary endpoint is the reoperation for any cause (excluding trauma) on the lumbar spine. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05277818
Study type Observational [Patient Registry]
Source SC Medica
Contact Aurélie MULLER
Phone +33 3 88 23 71 04
Email dpo@sc-medica.com
Status Recruiting
Phase
Start date September 7, 2022
Completion date March 15, 2027
View Details
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