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Osteonecrosis clinical trials

View clinical trials related to Osteonecrosis.

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NCT ID: NCT04103944 Completed - Osteonecrosis Clinical Trials

A Novel Reconstruction Device for Osteonecrotic Femoral Head Efficacy Evaluation

Start date: June 1, 2014
Phase: N/A
Study type: Interventional

Numerous studies describing surgical treatments to preserve hip replacements has several controversies and none of these procedures are universally accepted nor have compelling evidence for osteonecrosis of the femoral head (ONFH). With developing a newly approach osteonecrotic device surgical procedure to support the regeneration of necrotic bone and articular cartilage in vivo, this will be the first randomized-controlled feasibility study to determine its safety in ONFH patients.

NCT ID: NCT04079127 Completed - Clinical trials for Rheumatoid Arthritis

Avenir Müller Hip Stem Post Market Surveillance Study

Start date: January 9, 2010
Phase:
Study type: Observational

This study is a Post Market Clinical Follow up study to fulfil the post market surveillance obligations according to Medical Device Directive and European Medical Device Vigilance System (MEDDEV) 2.12-2. The data collected from this study will serve the purpose of confirming safety and performance of the Avenir Müller Hip Stem.

NCT ID: NCT04079114 Terminated - Clinical trials for Rheumatoid Arthritis

Post Market Clinical Follow-Up of the Zimmer Stafit Acetabular System

Start date: April 28, 2011
Phase:
Study type: Observational

This study is a Post Market Clinical Follow up study to fulfil the post market surveillance obligations according to Medical Device Directive and European Medical Device Vigilance System (MEDDEV) 2.12-2. The data collected from this study will serve the purpose of confirming safety and performance of the Zimmer Stafit Acetabular System.

NCT ID: NCT04072055 Terminated - Clinical trials for Osteo Arthritis Knee

MOTO Post-marketing Surveillance Study

Start date: September 25, 2019
Phase:
Study type: Observational

The prospective, multicentric, observational study has the aims to monitor the performance of the MOTO medial unicompartmental knee system in the treatment of patients with knee disease requiring a UKA. 150 patients will be recruited in 18 months and will be reviewed until 5 years follow-up visit after surgery. The primary objective of the study is to evaluate the prosthesis survival at 5 years.

NCT ID: NCT04012320 Completed - Children Clinical Trials

Efficacy and Safety on the Use of Bisphosphonates in Paediatrics

Bisphosphonate
Start date: October 31, 2018
Phase:
Study type: Observational

The investigators suppose that the impact of bisphosphonate therapy is beneficial on the bone during the growth period with few adverse events.

NCT ID: NCT04007783 Recruiting - Quality of Life Clinical Trials

Validation of the O-bridge Protocol: a Prospective, Multicenter Trial

Start date: March 4, 2017
Phase:
Study type: Observational

Surgical reconstruction to restore oral function and aesthetics after major ablative surgery in the oral cavity forms a challenge to maxillofacial surgeons, and greatly impacts patient' quality of life (QOL). The "Oncological-bridge (O-bridge®)" protocol, which offers (immediate/delayed) fixed prosthetic rehabilitation in a minimum of sessions and a strongly reduced two-week treatment time.

NCT ID: NCT03787329 Recruiting - Bone Marrow Clinical Trials

Autologous Bone Marrow Concentration for Avascular Necrosis of Femoral Head

Start date: April 14, 2017
Phase:
Study type: Observational

This study aims to evaluate the effect of bone marrow concentration on avascular necrosis of femur head by comparing clinical and imaging outcomes between patients receiving core decompression surgery with intraoperative bone marrow concentration and those receiving core decompression surgery only.

NCT ID: NCT03753282 Withdrawn - Clinical trials for Avascular Necrosis of the Femoral Head

Outcome After Avascular Necrosis of the Femoral Head in Young Patients

AVN
Start date: January 30, 2019
Phase:
Study type: Observational

1. The course of AVN between Initial diagnosis and total hip replacement (THA) is analysed. The impact of early interventions versus conservative therapy in AVN before THA will be evaluated. 2. The short and long term outcomes of AVN patients undergoing THA with respect to complications, reoperations and quality of life are investigated. Potential risk factors for adverse outcomes will be investigated.

NCT ID: NCT03735173 Completed - Shoulder Pain Clinical Trials

Comparing the Outcome of Cemented All-Polyethylene Pegged vs. Keeled Components Through a Subscapularis Tenotomy or a Subscapularis Peel

Start date: December 1, 2018
Phase: N/A
Study type: Interventional

Participants who choose to participate in this study, will either have their tendon repaired to tendon, so-called tenotomy repair, or tendon repaired to bone, so-called peel repair.

NCT ID: NCT03666637 Completed - Avascular Necrosis Clinical Trials

Femoral Neck Fracture in Adult and Avascular Necrosis and Nonunion

Start date: September 15, 2017
Phase:
Study type: Observational

One of the most serious sequelae of femoral neck fractures (FNFs) is avascular necrosis (AVN) and nonunion, and this translates to a significant morbidity and mortality. This study was conducted to determine the relationship between the etiologies and management of FNFs in our institution and its relationship to the development of AVN or nonunion.