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Clariance ErYs Registry

NCT05170815 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 760

Last updated 2026-03-17

No results posted yet for this study

Summary

International, prospective, single arm, multicenter and observational Post-Market Clinical Follow-up (PMCF).

The overall objective of this study is to collect preoperative, intraoperative and postoperative (at 9 weeks, 6 months, 1 year and 2 years) data on the clinical complications and functional outcomes of the study devices to demonstrate safety and performance in a real-world setting.

The primary objective is to demonstrate that the use of the study devices is safe.

The secondary objective is to demonstrate that the use of the study devices decreases the pain, and improves the quality of life and the daily activities of the subjects.

Conditions

  • Spine Degeneration
  • Spine Spondylosis Thoracic
  • Spinal Deformity
  • Spinal Tumor
  • Spinal Fracture

Interventions

PROCEDURE

Spine surgery

Implantation of spine Interbody Fusion Devices and/or Posterior fixation System.

Sponsors & Collaborators

  • Clariance

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-17
Primary Completion
2028-12-31
Completion
2028-12-31
FDA Device
Yes

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 NCT05170815 on ClinicalTrials.gov