MedTrace Logo

Safety and Efficacy of the CarboFix Pedicle Screw System

NCT02039232 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46

Last updated 2019-04-17

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety and efficacy of CarboFix' Pedicle Screw System in the lumbar spine.

Conditions

  • Degenerative Disc Disease
  • Spondylolisthesis
  • Spinal Stenosis
  • Spinal Curvatures
  • Tumor

Interventions

DEVICE

Pedicle screw system

Sponsors & Collaborators

  • CarboFix Orthopedics Ltd.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2017-08-31
Completion
2018-02-28

Countries

  • Israel

Study Locations

More Related Trials

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 NCT02039232 on ClinicalTrials.gov