At a glance
ClinicalIndex Comparison RecordN/ACompleted· 57 enrolled
Drug / intervention
Implantation of the CarboClear Pedicle Screw Systemdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
CarboClear Pedicle Screw System
In Brief
A clinical study evaluating Implantation of the CarboClear Pedicle Screw System for Degenerative Disc Disease and Spondylolisthesis, Grade 1. Completed, enrolled 57 participants across 8 sites in 2 countries.
Detailed Summary
The purpose of this trial is to demonstrate the safety and effectiveness of the CarboClear Pedicle Screw System, for skeletally mature DDD patients undergoing one level spinal fusion in combination with interbody fusion device, and requiring immediate, rigid, posterior spinal stabilization of the lumbar and/or sacral spine.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesIsrael, United States
CollaboratorsCarboFix Orthopedics Inc.
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedDec 2015
Enrollment StartDec 2015
Primary CompletionDec 2022
TodayJul 2026
First PostedDec 10, 2015
Enrollment StartDec 27, 2015
Primary CompletionDec 28, 2022
TodayJul 2, 2026
Enrollment to primary: 7.0 yearsPosted 10.6 years ago
Interventions
Implantation of the CarboClear Pedicle Screw Systemdevice