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Necrosis clinical trials

View clinical trials related to Necrosis.

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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: NCT02162186 Completed - Avascular Necrosis Clinical Trials

Clinical and Radiographic Outcomes of the Corin Tri-Fit Total Hip Replacement

Start date: October 2014
Phase:
Study type: Observational

The study will evaluate the radiographs (x-rays) of 100 patients with a TriFIT total hip at 2 weeks, 3 months, 6 months, 12 months, and yearly following surgery to see if there has been any movement or wear in the hip stem over the course of the study. The study will also record clinical data on each patient using various functional tests and questionnaires at the same intervals.

NCT ID: NCT02160132 Recruiting - Clinical trials for Glomerulonephritis, IGA

A Controlled Study of Steroids Therapy for Patients of IgA Nephropathy With Active Pathological Changes.

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

This prospective, randomized, controlled, multi-center clinical trial will evaluate the effect and security of steroids therapy for patients of IgA nephropathy with active pathological changes,including crescents,necrosis and microthrombus.

NCT ID: NCT02145130 Completed - Scars Clinical Trials

Phase I Study for Autologous Dermal Substitutes and Dermo-epidermal Skin Substitutes for Treatment of Skin Defects

Start date: May 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is the evaluation of the safety of autologous tissue-engineered dermal substitutes "denovoDerm" (first arm) and dermo-epidermal skin substitutes "denovoSkin" (second arm) transplanted onto the wound bed in children and adults.

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: NCT02096211 Active, not recruiting - Osteoarthritis Clinical Trials

Ceramic-on-Ceramic (COC) 36mm Acetabular Bearing Insert Post Approval Study-New Subjects (COC36mmPAS)

COC36mmPAS
Start date: June 1, 2014
Phase:
Study type: Observational

This study is intended to gather short (Pre-operative to 4-years) and mid-term (5-years) information regarding the performance and safety of the commercially available 36mm CERAMAX® Ceramic on Ceramic Total Hip System from a cohort of new study subjects that were not previously involved in the IDE study for this device.

NCT ID: NCT02096198 Completed - Osteoarthritis Clinical Trials

Ceramic On Ceramic (COC) 36mm PAS IDE Rollover Subjects; Ceramic Acetabular Bearing With Ceramic Femoral Head in Total Hip Replacement

COC36mmPAS
Start date: January 1, 2014
Phase:
Study type: Observational

This study is intended to gather medium (5- to 7-years) and long-term (minimum 8- to 10-years) information regarding the performance and safety of the commercially available 36mm CERAMAX® Ceramic on Ceramic (COC) Total Hip System from a cohort of study subjects that were previously enrolled in the IDE study. (COC = 36mm ceramic acetabular bearing insert component that articulates with a ceramic femoral head in the COC total hip replacement system)

NCT ID: NCT02092467 Completed - Clinical trials for Arthritis, Rheumatoid

Safety Study Of Tofacitinib Versus Tumor Necrosis Factor (TNF) Inhibitor In Subjects With Rheumatoid Arthritis

Start date: March 14, 2014
Phase: Phase 4
Study type: Interventional

This post-marketing study is designed to compare the safety of tofacitinib versus TNF inhibitor with respect to major cardiovascular adverse events and malignancies, excluding non-melanoma skin cancers when given to subjects with rheumatoid arthritis. Other safety events, including non-melanoma skin cancers, hepatic events, infections, and efficacy parameters will be collected and evaluated in the study.

NCT ID: NCT02087449 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

Evaluate E1 Wear, Clinical Performance of E1 Liner in THA in Korean Patient Population

E1Hip
Start date: February 2013
Phase:
Study type: Observational

Evaluate E1 wear, Clinical Performance of E1 liner in THA in Korean Patient Population