Non-Interventional Study to Evaluate Safety and Efficacy of NOVOCART 3D in Patients With Cartilage Defects
NCT02348697 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 81
Last updated 2019-12-03
Summary
Non-interventional study to evaluate safety and efficacy of NOVOCART 3D in adult and adolescent patients with full thickness cartilage defects after the treatment with NOVOCART 3D.
Conditions
- Cartilage Diseases
Interventions
- BIOLOGICAL
-
NOVOCART 3D
Autologous Chondrocyte Implantation
Sponsors & Collaborators
-
Aesculap AG
collaborator INDUSTRY -
Tetec AG
lead INDUSTRY
Principal Investigators
-
Alexandra Kirner, PhD · TETEC AG Reutlingen
Eligibility
- Min Age
- 14 Years
- Max Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-06-30
- Primary Completion
- 2019-10-30
- Completion
- 2019-10-30
Countries
- Germany
Study Locations
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