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A Feasibility Study to Evaluate the TURRIS Facet Fusion System in Lumbar Spinal Surgery

NCT02294669 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3

Last updated 2022-04-04

No results posted yet for this study

Summary

This is a prospective, exploratory study to verify intra-operative handling and safety and to collect preliminary short-term safety and efficacy data of the Turris® Facet Fuser, a small bioresorbable device for the immediate immobilization of the facet joint.

Patients eligible for study enrollment will present with degenerative lumbar spinal diseases involving the L4/L5 segment and requiring spinal fusion.

Conditions

  • Spinal Disease

Interventions

DEVICE

Turris Facet Fuser

Study participants will have a Turris Facet Fuser inserted into the contralateral facet joint, instead of a state of the art contralateral pedicle screw system.

Sponsors & Collaborators

  • ISS integrated Scientific Services AG

    collaborator UNKNOWN

  • SpineWelding AG

    lead INDUSTRY

Principal Investigators

  • Ulrich Berlemann, MD · Rückenzentrum Oberaargau

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-02-28
Primary Completion
2016-06-18
Completion
2016-06-18

Countries

  • Switzerland

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 NCT02294669 on ClinicalTrials.gov