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Single Center Study Comparing MOBIS II ST vs MOBIS PEEK

NCT02852187 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2020-03-19

No results posted yet for this study

Summary

Prospective randomized clinical study comparing SIGNUS MOBIS PEEK vs SIGNUS MOBIS II ST in patients with Degenerative Disc Disease at one or two contiguous levels from L2-S1

Conditions

  • Lumbar Disc Disease

Interventions

DEVICE

SIGNUS MOBIS PEEK Cage

Lumbar Interbody Fusion

DEVICE

SIGNUS MOBIS II ST Cage

Lumbar Interbody Fusion

Sponsors & Collaborators

  • Signus Medizintechnik GmbH

    lead INDUSTRY

Principal Investigators

  • William F. Lavelle, MD · Upstate Orthopedics

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2016-07-31
Primary Completion
2018-11-30
Completion
2018-11-30

Countries

  • United States

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 NCT02852187 on ClinicalTrials.gov