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Necrosis clinical trials

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NCT ID: NCT00578994 Completed - Osteoarthritis Clinical Trials

A Clinical Investigation of the Oxford® Meniscal Unicompartmental Knee System

Start date: March 2006
Phase:
Study type: Observational

The purpose of this study is to collect information on complications and survivorship of patients implanted with the Oxford™ Meniscal Unicompartmental Knee System at multiple sites in the United States.

NCT ID: NCT00578851 Completed - Osteoarthritis Clinical Trials

A Clinical Investigation of the C2a-Taper™ Acetabular System

Start date: April 2006
Phase: N/A
Study type: Observational

The objective of this study is to gather clinical and survivorship information for the C2a-Taper™ Acetabular System, a ceramic-on-ceramic hip articulating system.

NCT ID: NCT00546598 Terminated - Osteoarthritis Clinical Trials

Post-approval Study of the DURALOC® Option Ceramic-on-Ceramic Hip Prosthesis System

Start date: January 1, 2006
Phase: Phase 4
Study type: Interventional

This study is being conducted to gather medium and long-term information regarding the performance and safety of the commercially available DURALOC® Option Ceramic-on-Ceramic Hip Prosthesis System.

NCT ID: NCT00509704 Completed - Renal Cell Cancer Clinical Trials

Influence of Sutent on Tumor Vascularization and Necrosis in Patients With Renal Cell Carcinoma

Start date: October 2008
Phase: N/A
Study type: Observational

The purpose of the study is to assess the effect of Sunitinib on tumor vascularization and necrosis in patients with metastatic renal cell cancer.

NCT ID: NCT00472173 Completed - Clinical trials for Dental Pulp Necrosis

Assessment of a New Apexification Method for Patients Presenting a Non Vital Immature Tooth

APEXMTA
Start date: May 2007
Phase: Phase 3
Study type: Interventional

Pulp necrosis is one of the main complication of dental trauma. When it happens on an immature tooth, pulp necrosis implies a lack of root maturation and apical closure. A therapy called apexification is required to induce the formation of a calcified apical barrier allowing a permanent and hermetic root filling.The aim of this study is to compare the efficacy of a new apexification method using Mineral Trioxide Aggregate (MTA®) with the reference treatment based on calcium hydroxide repeated stimulations.

NCT ID: NCT00412841 Terminated - Avascular Necrosis Clinical Trials

Atorvastatin to Prevent Avascular Necrosis of Bone in Steroid Treated Exacerbated Systemic Lupus Erythematosus

Start date: November 2002
Phase: Phase 2
Study type: Interventional

This study uses the cholesterol lowering drug atorvastatin, also known as lipitor, to show reduction of avascular necrosis in steroid treated lupus patients. Avascular necrosis is a disease resulting from the loss of blood supply to the bones which can cause the bone to collapse. The collapse of bone may require a surgical replacement of the joint and can be disabling for life. Avascular necrosis is presently not preventable but research has shown that lipid lowering drugs such as lipitor can reduce or prevent avascular necrosis in animals. We therefore hypothesize that lipitor will reduce the incidence of avascular necrosis in lupus patients taking high dose steroids.

NCT ID: NCT00393848 Completed - Osteoarthritis Clinical Trials

Effectiveness of Two Types of Treatment in Restoring Muscle After Hip or Knee Surgery

Start date: October 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effects of two postoperative interventions designed to preserve muscle protein after major hip or knee surgery.

NCT ID: NCT00306917 Terminated - Clinical trials for Rheumatoid Arthritis

Clinical Study Comparing Two Implant Surface Finishes in Patients Undergoing Cementless Total Hip Replacement

SPD
Start date: November 1, 2002
Phase: N/A
Study type: Interventional

Prospective, randomized study of Summit Porocoat versus Summit DuoFix HA in total hip arthroplasty

NCT ID: NCT00289107 Completed - Clinical trials for Rheumatoid Arthritis

Randomized Fixed Bearing vs Mobile Bearing Cruciate Substituting TKA

Start date: April 1, 2001
Phase: N/A
Study type: Interventional

The study will evaluate the clinical performance of the rotating platform and fixed bearing implants through patient questionnaires, outcomes scoring and radiographic assessment.

NCT ID: NCT00289094 Completed - Clinical trials for Rheumatoid Arthritis

Randomized Fixed Bearing vs Mobile Bearing Cruciate Retaining TKA

Start date: March 1, 2001
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the clinical performance of the rotating platform and fixed bearing implants in patients undergoing primary total knee replacement. Outcome scoring and radiographic assessment will be the methods used to evaluate performance.