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A Postmarket Surveillance Study of the Paradigm Spine Dynamic Stabilization System (DSS)

NCT01461005 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1

Last updated 2020-02-19

Study results available
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Summary

The purpose of the Post-Market Surveillance study is to evaluate safety.

Conditions

  • Spondylolisthesis
  • Neurologic Deficits
  • Kyphosis
  • Pseudarthrosis

Interventions

DEVICE

Dynamic Stabilization System (DSS)

Dynamic Stabilization System

Sponsors & Collaborators

  • MCRA

    collaborator INDUSTRY

  • Paradigm Spine

    lead INDUSTRY

Principal Investigators

  • Gitela Gandelman · Paradigm Spine LLC

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-09-30
Primary Completion
2016-09-30
Completion
2016-09-30

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 NCT01461005 on ClinicalTrials.gov