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Personalized Spine Study Group Registry

NCT03843476 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2020-09-29

No results posted yet for this study

Summary

As a registry, the primary objective of the study is a data collection initiative. The study will collect clinical and radiographic outcomes of patients implanted with Medicrea's PSR. The secondary objective is to collect clinical and radiographic outcomes of patients with Medicrea hardware as a control cohort to the patient-specific rods.

Conditions

  • Scoliosis; Adolescence
  • Degenerative Disc Disease
  • Spinal Fusion
  • Kyphoscoliosis
  • Pseudoarthrosis of Spine
  • Spinal Stenosis
  • Kyphoses, Scheuermann

Interventions

DEVICE

Patient Specific Rod

Posterior spinal fusion rod

Sponsors & Collaborators

  • Medicrea, USA Corp.

    lead INDUSTRY

Eligibility

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

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2020-09-30
Completion
2020-09-30
FDA Device
Yes

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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 NCT03843476 on ClinicalTrials.gov