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NCT00158613 · ClinicalTrials.gov registry record · Phase 4

Study of the Treatment of Articular Repair (STAR)

A Phase 4 study, sponsored by Vericel Corporation.

Completed
Registry status
Phase 4
Development phase
126
Enrollment target

NCT00158613 is a Phase 4 study that has completed, run by Vericel Corporation. The registered enrollment target is 126 participants.

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The verdict

NCT00158613, a Phase 4 study, has completed, sponsored by Vericel Corporation.

COMPLETED
Registry status
Phase 4
Development phase
126 participants
Enrollment target

Study 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.

Interventions

  • BIOLOGICAL Carticel (autologous cultured chondrocyte) implantation

Trial Details

FieldValue
Enrollment Target 126 participants
Start Date 2000-03
Est. Completion 2005-11
Phase Phase 4

Sponsor

Vericel Corporation

11 total trials

What the Registry Record Tells You About NCT00158613

The ClinicalTrials.gov registry entry for NCT00158613 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 126 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vericel Corporation, which has 11 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Carticel (autologous cultured chondrocyte) implantation is the first listed.

NCT00158613 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00158613 about?

NCT00158613 is a clinical study titled "Study of the Treatment of Articular Repair (STAR)". 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 ...

What is the current status of trial NCT00158613?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 126 participants. The study started on 2000-03. Estimated completion is 2005-11.

What interventions are being tested in trial NCT00158613?

The interventions under investigation include: Carticel (autologous cultured chondrocyte) implantation (BIOLOGICAL).

Who is sponsoring clinical trial NCT00158613?

This trial is sponsored by Vericel Corporation, which has 11 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.