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Active, not recruiting Observational

Comprehensive Nano - Post Market Clinical Follow-Up Study

NCT03423953 · tracked via the Priya Life Science South Korea tracker
Phase
Observational
Started
2013-10-30
Last updated
2026-04-21

Condition(s) studied

OsteoarthritisAvascular NecrosisRheumatoid ArthritisRevisionCorrection of Functional Deformity

Investigational drug(s) / intervention(s)

Comprehensive Nano

Comprehensive Nano: Patients requiring the Comprehensive Nano shoulder system.

Study summary

This data collection project is intended to provide clinical outcomes data to engineering, marketing as well as fulfill the post market surveillance requirements of various regulatory authorities. The study will be a prospective and one-arm.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis. * Rheumatoid arthritis * Revision where other devices or treatments have failed * Correction of functional deformity. * Difficult clinical management problems where other methods of treatment may not be suitable or may be inadequate * Difficult clinical management problems where other methods of treatment may not be suitable or may be inadequate Exclusion Criteria: * Infection * Sepsis * osteomyelitis

Primary outcome measure(s)

  • Survivorship — 10 years
    Kaplan Meier method

Trial sites (5)

FacilityCityRegionStatus
Privatklinik Leech Graz Styria
Kingston General Hospital Kingston Ontario
Chonnam National University Hospital Gwangju Gwangju
Samsung Medical Centre Seoul Seoul
University of Liverpool Liverpool Merseyside
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03423953 on ClinicalTrials.gov ↗ ← All trials in South Korea