Viewing Study NCT00158613



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Last Modification Date: 2024-10-26 @ 9:15 AM
Study NCT ID: NCT00158613
Status: COMPLETED
Last Update Posted: 2021-05-11
First Post: 2005-09-08

Brief Title: Study of the Treatment of Articular Repair STAR
Sponsor: Vericel Corporation
Organization: Vericel Corporation

Study Overview

Official Title: A Prospective Longitudinal Within-Patient Evaluation of the Effectiveness Durability of Carticel Autologous Cultured Chondrocytes Compared to Non-Carticel Surgical Treatment for Articular Cartilage Defects of the Knee
Status: COMPLETED
Status Verified Date: 2021-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study is a prospective longitudinal multi-center within patient evaluation of patients with articular cartilage defects of the knee who have had an inadequate response to a prior non-Carticel surgical treatment Patients who met eligibility criteria were enrolled in the study Subsequent to implantation with Carticel patients have follow-up every 6-months up to 48-months
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None