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Safety and Performance of a Hernia Blocking System

NCT04188236 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2023-10-18

No results posted yet for this study

Summary

Prospective, multi-center, single-arm clinical study to assess the performance of an Hernia Blocking System in preventing clinically symptomatic recurrent lumbar disc herniation.

Conditions

  • Disk Herniated Lumbar

Interventions

DEVICE

Hernia Blocking System

Hernia Blocking System device implanted during a lumbar discectomy procedure

Sponsors & Collaborators

  • NEOS Surgery

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-23
Primary Completion
2023-06-26
Completion
2023-06-26

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04188236 on ClinicalTrials.gov