Evaluation of an Acellular Osteochondral Graft for Cartilage LEsions Pilot Trial

PHASE2TerminatedINTERVENTIONAL
Enrollment

2

Participants

Timeline

Start Date

June 30, 2010

Primary Completion Date

December 31, 2013

Study Completion Date

May 31, 2014

Conditions
Articular Cartilage Injury
Interventions
DEVICE

Kensey Nash Corp. Cartilage Repair Device

To perform the Cartilage Repair Device implantation procedure, the surgeon first removes the damaged cartilage. Then, the surgeon creates a cylindrical hole in the bone below the area of damaged cartilage. The Cartilage Repair Device is then implanted into the hole so that the surface is level with the surrounding native cartilage. The Cartilage Repair Device will then absorb blood and bone marrow from the bone to begin the healing process.

PROCEDURE

Microfracture

To perform the microfracture technique, the surgeon will first remove the damaged cartilage. Then, the surgeon will make a number of small fractures in the bone below the area of damaged cartilage. The fractures cause the bone to bleed and a clot to form over the exposed bone. Over time, the clot forms a layer of fibrocartilage over the bone.

Trial Locations (2)

21804

Peninsula Orthopedic Associates, Salisbury

63122

U.S. Center for Sports Medicine, Kirkwood

Sponsors
All Listed Sponsors
lead

Kensey Nash Corporation

INDUSTRY

NCT01183637 - Evaluation of an Acellular Osteochondral Graft for Cartilage LEsions Pilot Trial | Biotech Hunter | Biotech Hunter