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Arthritis clinical trials

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NCT ID: NCT02348086 Recruiting - Clinical trials for Rheumatoid Arthritis

Outcomes Data of Adipose Stem Cells to Treat Rheumatoid Arthritis

Start date: January 2015
Phase:
Study type: Observational

The purpose of this study is to determine the impact that treatment with a cellular concentrate derived from an individual's own fat, known as the stromal vascular fraction (SVF), has on pain and functionality in people with rheumatoid arthritis (RA). SVF contains multiple cellular components, including stem cells, with both regenerative and anti-inflammatory properties. This therapy has shown promise for ameliorating the symptoms of RA. This study is designed to evaluate changes in pain and functionality in individuals with RA for up to 12 months following SVF treatment.

NCT ID: NCT02347384 Completed - Clinical trials for Rheumatoid Arthritis

Project JAY THA Registration Study

Start date: April 20, 2015
Phase: N/A
Study type: Interventional

This is a prospective, randomized, multicenter clinical study in Chinese subjects to compare the safety and efficacy of the Delta PLUS Femoral Head and SL-TWIN Stem with BIOLOX forte ball head and SL-PLUS Stem in total hip arthroplasty

NCT ID: NCT02346877 Terminated - Clinical trials for Persistence to Enbrel

Evaluate Effects of Personalized Patient Counselling for Enbrel® Therapy in Adults With Rheumatoid Arthritis

Start date: April 2015
Phase: Phase 4
Study type: Interventional

This study will evaluate whether the effect of personalized patient counselling tool, Information-Motivation-Strategy (IMS) based on the results of the Beliefs about Medicines Questionnaire (BMQ) will improve persistence of Enbrel (etanercept) therapy at week 52 in subjects with rheumatoid arthritis over the historical control as estimated by the standard of care.

NCT ID: NCT02343770 Recruiting - Clinical trials for Idiopathic Juvenile Arthritis

Biomarkers in Idiopathic Juvenile Arthritis

Start date: June 2015
Phase: N/A
Study type: Interventional

Juvenile idiopathic arthritis (JIA) is the most common form of arthritis in children. The etiology is unknown. Several types of arthritis fall under the JIA heading. Oligoarticular JIA with antinuclear antibodies affects about half of all children. There 's no specific markers. Our purpose is to identify new markers in this pathology. The ProtoArray®Human Protein Microarray allows rapid and efficient detection of protein interaction using a suitable protein or small molecule probe. The investigators hope so detect novel potential autoantigen biomarkers specific in JIA.

NCT ID: NCT02341391 Completed - Clinical trials for Degenerative Arthritis

Safety and Biological Efficacy Study of TisssueGene-C to Degenerative Arthritis

Start date: February 2007
Phase: Phase 1
Study type: Interventional

The primary purpose of the this study is to evaluate the safety of TissueGene-C, a gene therapy product that uses allogenic human chondrocytes expressing Transforming Growth Factor(TGF)-β1 by assessing the inflammation at the injection site, the incidence and severity of the adverse events, the physical examination findings, and the laboratory test results after the intra-articular injection of TissueGene-C. And Secondary purpose is to evaluate the biological efficacy (knee pain, range of motion, functional tests, and MRI) of TissueGene-C and the distribution of TissueGene-C outside the injection site.

NCT ID: NCT02341378 Completed - Clinical trials for Degenerative Arthritis

Efficacy and Safety Study of TissueGene-C to Degenerative Arthritis

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

To assess the efficacy and safety of the intra-articular injection of TissueGene-C in patients with degenerative arthritis of the knee

NCT ID: NCT02341066 Recruiting - Clinical trials for Rheumatoid Arthritis

Endothelial Dysfunction Evaluation for Coronary Heart Disease Risk Estimation in Rheumatoid Arthritis (EDRA Study)

EDRA
Start date: July 2015
Phase: N/A
Study type: Observational

To evaluate the contribution of the assessment of endothelial dysfunction (ED) in improving coronary hearth disease (CHD) risk stratification obtained by the Framingham risk score (FRS) in rheumatoid arthritis population (RA).

NCT ID: NCT02340390 Completed - Clinical trials for Rheumatoid Arthritis

G7 Acetabular System vs. Exceed ABT Acetabular System in THA

G7
Start date: May 2015
Phase: N/A
Study type: Interventional

Evaluate the safety and effectiveness of patients who received G7 Acetabular system in conjunction with Ceramic on Ceramic articulation and Taperloc Complete Microplasty stem compared to patients who received the Exceed ABT Acetabular system with the same combination

NCT ID: NCT02337244 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

Zimmer POLAR Persona - TKA (EMEA Study)

Start date: November 18, 2013
Phase:
Study type: Observational

The primary objective of this study is to obtain implant survivorship and clinical outcomes data for commercially available Persona knee implants used in primary total knee arthroplasty. The assessment will include: 1. Implant survivorship based on removal of a study device. 2. Safety based on incidence and frequency of adverse events. 3. Clinical performance measured by overall pain and function, quality of life data, radiographic parameters and survivorship.

NCT ID: NCT02336009 Recruiting - Clinical trials for Rheumatoid Arthritis

Patient Perceived Outcome After Total Wrist Arthroplasty With a New Total Wrist Arthroplasty Implant

Start date: October 2014
Phase: Phase 2/Phase 3
Study type: Interventional

Total wrist arthroplasty (TWA) surgery has developed gradually and can offer patients with rheumatoid arthritis/osteoarthritis reduced wrist pain with mainly preserved wrist range of movement. Each year 60-70 patients in Sweden are operated with a total wrist arthroplasty. Several implants are available on the market and they all have different pros and cons. One risk with a total wrist arthroplasty is loosening of the implant. If an implant is loose, revision of the implant to another TWA is sometimes possible, if not, a wrist fusion is the likely alternative. Revision rates five years after the index operation have improved, however, they cannot yet compare with the results after a total hip arthroplasty. A newly designed TWA has been developed by the department of Hand Surgery, Örebro university Hospital, Örebro, Sweden, in cooperation with Trimed Inc. The newly developed TWA offers theoretical advantages and has been biomechanically tested at the Mayo clinic. This is a pilot study where patients operated with the TWA will be assessed pre and postoperatively according to study protocol in order to evaluate outcome after TWA radiologically, clinically and regarding patient perceived outcome measures.