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Defect of Articular Cartilage clinical trials

View clinical trials related to Defect of Articular Cartilage.

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NCT ID: NCT02855073 Active, not recruiting - Knee Osteoarthritis Clinical Trials

Clinical Trial to Compare ReJoinTM to Sodium Hyaluronate Injection for Knee Osteoarthritis Cartilage Defects

Start date: July 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of ReJoinTM for the Knee Osteoarthritis patients with Cartilage Defects comparing to Sodium Hyaluronate Injection.

NCT ID: NCT02659215 Active, not recruiting - Clinical trials for Defect of Articular Cartilage

HyaloFAST Trial for Repair of Articular Cartilage in the Knee

FastTRACK
Start date: December 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of Hyalofast® scaffold with bone marrow aspirate concentrate (BMAC) compared to microfracture in the treatment of symptomatic cartilage defects of the knee.

NCT ID: NCT02539030 Active, not recruiting - Osteoarthritis Clinical Trials

Comparison of Efficacy and Safety of Microfracture and Modified Microfracture

Start date: February 2013
Phase: Phase 4
Study type: Interventional

This study was designed to evaluate the efficacy and safety of a modified microfracture using collagen, and to compare them with those of a simple microfracture to prove the non-inferiority of the modified microfracture using collagen in patients with cartilage defects in their knees.

NCT ID: NCT02537067 Active, not recruiting - Clinical trials for Defect of Articular Cartilage

Efficacy and Safety of Chondron (Autologus Chondrocyte) in Patients With Cartilage Defects in Their Ankle

Start date: January 2010
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the efficacy and safety of Chondron (Autologus Chondrocyte) in patients with cartilage defects in their ankle for 18 months

NCT ID: NCT02524509 Active, not recruiting - Clinical trials for Defect of Articular Cartilage

the Safety and Efficacy Evaluation of Chondron Compared With Mircrofracture of Knee

Start date: January 2012
Phase: Phase 4
Study type: Observational

The purpose of this study is to evaluate safety and efficacy of Chondron(autologous cultured Chondrocyte) by comparing between Chondron implantation and Microfracture.

NCT ID: NCT01670617 Active, not recruiting - Knee Injuries Clinical Trials

DeNovo NT Natural Tissue Graft Stratified Knee Study

Start date: March 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the long-term relief of pain and return to function for patients receiving DeNovo NT for cartilage lesions in the knee. DeNovo NT is a marketed product and has been used in more than 7,500 patients over the last 7 years.

NCT ID: NCT01347892 Active, not recruiting - Clinical trials for Osteochondritis Dissecans

DeNovo NT Ankle LDC Study

Start date: March 2011
Phase: N/A
Study type: Observational

The purpose of this post-market clinical study is to collect long-term outcomes for DeNovo NT Graft treatment of articular cartilage lesions in the ankle in a standard clinical setting. Outcomes to be assessed include pain, function, activity levels and healthcare resource use.

NCT ID: NCT00885729 Active, not recruiting - Clinical trials for Defect of Articular Cartilage

Mesenchymal Stem Cells in a Clinical Trial to Heal Articular Cartilage Defects

Start date: April 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to: - Compare the treatment efficacy of autologous mesenchymal stem cells (Mesenchymal Stem Cells) versus chondrocytes implanted in a commercial available scaffold in a human clinical trial. - Determine the effects of specific three months strength training program preoperatively to improve knee function and possible postpone the need of cartilage repair surgery. - Determine if degenerative changes occur in the knee joints following cartilage repair. This question will be investigated in the proposed clinical trial. - Determine the characteristics of patients treated either by surgery or by rehabilitation in a long-term follow-up (1, 5 years).