PASS MIS® Post-market Clinical Follow-up

NCT02931266 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 5

Last updated 2023-05-06

No results posted yet for this study

Summary

Prospective, multicenter non comparative and observational study (post-market clinical follow-up).

Conditions

  • Spinal Fractures

Interventions

DEVICE

PASS MIS®

Posterior mini-invasive osteosynthesis

Sponsors & Collaborators

  • Medicrea International

    lead INDUSTRY

Principal Investigators

  • Stephane Fuentes, MD · Hopital la Timone, Marseille

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2018-01-31
Completion
2018-01-31

Countries

  • France

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 NCT02931266 on ClinicalTrials.gov