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Osteonecrosis clinical trials

View clinical trials related to Osteonecrosis.

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NCT ID: NCT02198001 Recruiting - Clinical trials for Bisphosphonate-Associated Osteonecrosis of the Jaw

Prospective Randomized Study: Assessment of PRF Efficacy in Prevention of Jaw Osteonecrosis After Tooth Extraction

PRF
Start date: January 2014
Phase: N/A
Study type: Interventional

This prospective study will include patients taking or having taken bisphosphonates and needing dental extractions. The aim of this study is to validate the contribution of PRF (Platelet Rich Fibrin) in tooth extraction sites. In the test group (PRF) and in the control group (no PRF), we use the same atraumatic extraction protocol associated with the same antibiotic procedure.

NCT ID: NCT02170545 Completed - Avascular Necrosis Clinical Trials

CT Imaging Evaluation of Humerus Fractures

Start date: March 2014
Phase:
Study type: Observational

Displaced, multi-part intracapsular, proximal humerus fractures represent a major challenge for patients and orthopedic surgeons. Proximal humerus fractures represent the third most common fracture after hip and distal radius fractures, and more than 20% of these fractures meet operative indications. Unfortunately, one of the major complications of these fractures is the development of avascular necrosis (AVN), or death of the bone as a result of the loss of blood supply to it. Currently, the ability to predict AVN is limited. The purpose of this study is to determine if computed tomography imaging can identify a quantifiable predictor of AVN following this type of humeral fracture.

NCT ID: NCT02139345 Completed - Clinical trials for Rheumatoid Arthritis

TC-A Registration Study

Start date: September 23, 2014
Phase: N/A
Study type: Interventional

This is a prospective, randomized, multicenter clinical study to compare the safety and efficacy of TC-A PS total knee system with TC-PLUS Solution PS total knee system in Chinese subjects.

NCT ID: NCT02114489 Terminated - Hip Necrosis Clinical Trials

Study Comparing Ibandronate Versus Placebo in Hip Osteonecrosis

Start date: June 2014
Phase: Phase 3
Study type: Interventional

Aseptic osteonecrosis of the hip (AOH) concern 1 Swiss young adult to 1000 (30-40 years old). They are responsible to a severe joint destruction and in the majority of cases a joint replacement. To the hip, we can distinguish 4 stages of osteonecrosis according to Ficat: 1, 2, 3, 4. Stage 3 and 4 AOH management are unanimous surgical. But management of stage 1 and 2 are unclear. Bisphophonates are mainly used for bone and osteoporosis diseases. They decrease the bone turn over, and the risk of fracture. They also decrease the bone marrow oedema and the pain associated to this oedema. Ibandronate is a bisphosphonate with a rapid effect, a short half-life, easy to manage, and with few side effects. We designed a double-blind prospective randomized trial aiming to evaluate the efficacy of an infusion of ibandronate versus placebo on pain and AOH progression in patients with stage 1 and 2 AOH. Our hypothesis is that there will be a pain reduction >=20 mm on the VAS scale (SD 10mm) in the ibandronate group versus placebo, and a non radiological progression in the treated group.

NCT ID: NCT02077647 Completed - Clinical trials for Osteoarthritis, Knee

Focused Registry on the Conservative Treatment of Osteoarthritis of the Knee

Start date: March 2014
Phase:
Study type: Observational [Patient Registry]

The primary objective of this registry is to assess the functional outcome measured with the Knee Injury and Osteoarthritis Outcome Score (KOOS) for patients with medial unicompartmental osteoarthritis and osteonecrosis of the knee treated conservatively. The aim of the Focused Registry is to complete the data collection and enable a sound analysis for the Tomofix Small size study.

NCT ID: NCT02069340 Withdrawn - Malignant Neoplasm Clinical Trials

Genetics in Predicting Risk of Bisphosphonate-Related Osteonecrosis of the Jaw in Patients With Cancer Receiving Zoledronic Acid

Start date: June 2016
Phase: N/A
Study type: Interventional

This randomized clinical trial studies genetics in predicting risk of bisphosphonate-related osteonecrosis of the jaw in patients with cancer receiving zoledronic acid. Zoledronic acid is an anti-resorptive drug used as part of cancer treatment. A serious side effect of these drugs is death of the jawbone, commonly called bisphosphonate-related osteonecrosis of the jaw (BRONJ). Genetic research may help doctors understand risk factors for BRONJ or who is more likely to get BRONJ and why.

NCT ID: NCT02065167 Completed - Clinical trials for Avascular Necrosis of the Femoral Head

Evaluation of Mesenchymal Stem Cells to Treat Avascular Necrosis of the Hip

ORTHO-2
Start date: February 2014
Phase: Phase 2
Study type: Interventional

The purpose is to assess the safety and feasibility of cellular therapy derived from bone marrow, to help bone healing in patients with avascular necrosis of the hip.

NCT ID: NCT02007915 Terminated - Clinical trials for Femoral Head Avascular Necrosis

The Use of Bisphosphonates in the Treatment of Avascular Necrosis of the Femoral Head

Start date: July 2009
Phase: N/A
Study type: Interventional

To determine the safety and effectiveness of pamidronate in patients with radiographically proven avascular necrosis which are the result of unstable (acute) slipped capital femoral epiphysis, traumatic proximal femur fractures, traumatic hip dislocations, or idiopathic in nature.

NCT ID: NCT01998607 Completed - Solid Tumours Clinical Trials

Survey of XGEVA® Presrcibers in Europe to Evaluate Their Knowledge of the Summary of Product Characteristics Pertaining to Osteonecrosis of the Jaw

Start date: February 4, 2013
Phase: N/A
Study type: Observational

Osteonecrosis of the Jaw (ONJ) is an adverse effect of antiresorptive therapy that is well-recognized in patients with advanced cancer. Detailed information regarding this risk is specified in the Summary of Product Characteristics (SPC). The statements in the SPC are the most important mechanism for minimizing the risk for ONJ. The study objective is to measure the knowledge of oncology practitioners prescribing XGEVA® regarding the content pertaining to ONJ in the SPC after commercial availability.

NCT ID: NCT01979666 Terminated - Clinical trials for Necrosis, Avascular, of Bone

Nitrate Patch Use as Treatment of Knee AVN

Start date: January 2014
Phase: N/A
Study type: Interventional

The pathogenesis of AVN includes a defective blood supply to the knee joint. Local nitrates induce peripheral vasodilation and may improve blood supply to the affected tissue. This study aims to test whether the use of a nicotine patch may accelerate the healing process from AVN of the knee.