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Osteonecrosis clinical trials

View clinical trials related to Osteonecrosis.

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NCT ID: NCT00939900 Completed - Clinical trials for Avascular Necrosis of Femoral Head

Efficacy of Zoledronic Acid in Preventing Collapse of the Osteonecrotic Femoral Head

EZAPCOFH
Start date: July 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the effect of zoledronic acid over 2 years in preventing early collapse and progression of joint dome depression (≥ 2 mm by X-ray) of the femoral head in patients with large (> 30%: criteria according to Kim et al) nontraumatic osteonecrosis.

NCT ID: NCT00913679 Completed - Osteonecrosis Clinical Trials

A Comparison of Two Different Surgical Techniques in Hip Resurfacing Arthroplasty

Start date: November 1, 2008
Phase: N/A
Study type: Interventional

The purpose of the study is to compare two different surgical techniques in hip resurfacing arthroplasty (RHA), comparing bloodflow and metabolism in the femoral head, as well as implant migration, periprosthetic bone mineral density, gait function and patient recovery.

NCT ID: NCT00874211 Completed - Breast Cancer Clinical Trials

S0702: Osteonecrosis of the Jaw in Patients With Cancer Receiving Zoledronic Acid for Bone Metastases

Start date: December 2008
Phase:
Study type: Observational

RATIONALE: Gathering information about how often osteonecrosis of the jaw occurs in patients receiving zoledronic acid for bone metastases may help doctors learn more about the disease and provide the best follow-up care. PURPOSE: This clinical trial is studying osteonecrosis of the jaw in patients with cancer who are receiving zoledronic acid for bone metastases.

NCT ID: NCT00858585 Completed - Breast Cancer Clinical Trials

Genetic Risk of Osteonecrosis of the Jaw (ONJ) in Patients With Metastatic Cancer: Concordance Study

Start date: March 2009
Phase:
Study type: Observational

This study will examine genes in three different tissues and look for similarities and differences between normal cells and cancer cells. The tissues to be studies come from blood, lymph node and cancer.

NCT ID: NCT00833430 Terminated - Avascular Necrosis Clinical Trials

Avascular Necrosis (AVN) Long-Term Follow-up

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

Long-term follow-up of IDE patients for publication

NCT ID: NCT00821470 Completed - Necrosis Clinical Trials

Treatment of Osteonecrosis of the Femoral Head by Bone Marrow Transplantation

Start date: January 1999
Phase: Phase 1
Study type: Interventional

Aseptic non traumatic osteonecrosis (ON) is a painful disorder of the hip which often leads, in its final stage, to femoral head collapse and subsequent total hip replacement. Core decompression of the hip is the most widespread procedure used to treat early stage ON of the femoral head. Notwithstanding the fact that this procedure has been employed for more than three decades (2), its efficacy remains controversial (3;4). Recently, one suggested that ON might be a disease of bone cells and/or of mesenchymal cells. The levels of activity and the number of mesenchymal stem cells in both the hematopoietic and in the stromal compartments of the bone marrow have been shown to be depressed in patients with ON of the femoral head (9). The investigators have showed previously that the capacity of osteoblastic cells to replicate was decreased in the proximal femur of patients with ON of the femoral head (10). This finding raised the possibility that bone marrow containing stromal cells which have many of the characteristics of stem cell for mesenchymal tissues including bone could be implanted into the necrotic lesion of the femoral head.

NCT ID: NCT00813267 Active, not recruiting - Clinical trials for Osteochondritis of the Femoral Head

Mesenchymal Stem Cell for Osteonecrosis of the Femoral Head

Start date: December 2009
Phase: Phase 0
Study type: Interventional

Mesenchymal Stem Cells (MSCs) have been shown to have immunosuppressive and repairing properties. Bone marrow mononuclear cells (BMMNCs) have revascularization properties and complimentary effects to MSCs. The investigators will infuse expanded autologous MSCs and BMMNCs into patients with osteonecrosis of the femoral head. The study purpose is to examine whether this treatment will result in improvement in osteonecrosis of the femoral head.

NCT ID: NCT00781261 Recruiting - Osteonecrosis Clinical Trials

Osteonecrosis of the Hip and Bisphosphonate Treatment

BONES
Start date: August 2009
Phase: Phase 2
Study type: Interventional

Osteonecrosis of the hip is an important cause of musculoskeletal disability and finding therapeutic solutions has proven to be challenging. Osteonecrosis means death of bone which can occur from the loss of the blood supply or some other means. Although any age group may develop osteonecrosis, most patients are between 20 and 50 years old. The most common risk factor is a history of high steroid treatment for some medical condition. The next most common associated condition is a history of high alcohol use. There are some cases of osteonecrosis that occur in patients that are otherwise completely healthy with no detectable risk factors. In the earliest stage of the disease, x-rays appear normal and the diagnosis is made using MRI. The advanced stages of osteonecrosis begin when the dead bone starts to fail mechanically through a process of microfractures of the bone. As the disease progresses, the surface begins to collapse until, finally the integrity of the joint is destroyed. A wide range of surgical treatments with variable success rates have been proposed for the treatment of the osteonecrosis to preserve joint integrity, including core decompression, whereby the venous hypertension that ensues is lessened and revascularisation may be induced leading to bone repair. Nonsurgical treatment options are limited and usually result in a poor prognosis. Early stage disease can be treated with protected weight bearing and physiotherapy, however some studies have shown protected weight bearing to be associated with a greater than 85% rate of femoral head collapse. Unfortunately most studies indicate that the risk for disease progression is greater with nonsurgical treatment than with surgical intervention. There are no established pharmaceuticals for the prevention of treatment of osteonecrosis. Evidence is increasing that the nitrogen containing bisphosphonates may be beneficial in the treatment of osteonecrosis. One bisphosphonates (alendronate) has been evaluated in 60 patients diagnosed with osteonecrosis of the hip. Recent clinical studies have shown very promising results. All patients had symptomatic improvement after one year. Although the follow up time ranged from 3 months to 5 years, only 6 patients progressed to the point of needing surgery.

NCT ID: NCT00722007 Completed - Clinical trials for Rheumatoid Arthritis

Cormet Post-PMA Study: New Enrollment

PASNew
Start date: April 24, 2008
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the performance of the Cormet Hip Resurfacing implant system in the post-approval environment.

NCT ID: NCT00721994 Completed - Clinical trials for Rheumatoid Arthritis

Post-PMA Approval Study: 10 Year Follow-Up IDE Subjects

PAS:IDE
Start date: May 2008
Phase:
Study type: Observational

primary endpoint of this Study is maintenance of "at least good clinical status" for a period of 10 years following initial implantation among Cormet procedures enrolled inthe pre-market IDE.