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Joint Diseases clinical trials

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NCT ID: NCT01265264 Completed - Arthritis Clinical Trials

Study to Evaluate sUA Lowering Activity, Safety and Efficacy of Oral Ulodesine Added to Allopurinol

Start date: December 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether ulodesine and allopurinol combined for 12 weeks are effective in treating gout in patients who are not adequately responding to allopurinol alone.

NCT ID: NCT01256216 Completed - Joint Disease Clinical Trials

Signature Versus Computer Assisted Surgery Study

Start date: September 2010
Phase: N/A
Study type: Interventional

The purpose of the data collection is to document the performance and clinical outcomes of the Vanguard Knee using Signature Custom Cutting Guides and Computer Assisted Surgery.

NCT ID: NCT01246674 Completed - Clinical trials for Osteoarthrosis Patients With Total Hip Arthroplasty

Thigh Swelling, Hip-muscle Strength, and Functional Performance Following Total Hip Arthroplasty

THA
Start date: January 2011
Phase: N/A
Study type: Observational

By this study the investigators wish to (1) quantify hip strength and functional-performance deficits at discharge after fast-track total hip arthroplasty (THA), and (2) investigate if changes in thigh circumferences, or hip pain are correlated to changes in hip strength and functional-performance after fast-track THA.

NCT ID: NCT01232634 Completed - Hemophilia Clinical Trials

Validation of Ultrasound as a Diagnostic Tool for Assessment of Hemophilic Arthropathy of Knees and Ankles

Start date: September 2010
Phase: Phase 2
Study type: Observational

The purpose of this study is to test the external validity of the systemic ultrasound protocol for data acquisition and interpretation, in order to diagnose soft tissue and osteochondral abnormalities in hemophilic children.

NCT ID: NCT01227694 Completed - Clinical trials for Osteoarthritis, Knee

Adult Stem Cell Therapy for Repairing Articular Cartilage in Gonarthrosis

Start date: October 2010
Phase: Phase 1/Phase 2
Study type: Interventional

This is a prospective, open-label, single-dose, single-arm phase I-II study in which 15 patients diagnosed with gonarthrosis grade II-III (Kellgren and Lawrence) will enter the study with the primary objective of assessing the feasibility and safety of the knee articular infiltration of autologous bone marrow mesenchymal stem cells (MSC). Secondary objectives are to assess the efficacy by imaging procedures and clinical questionnaires. MSC obtained from each patient's bone marrow will be isolated and expanded "Ex-Vivo" under GMP conditions at Xcelia-División de Terapias avanzadas del Banc de Sang I Teixits. After 21 days, patients will be implanted a single-dose of approximately 40 millions of autologous MSC in the knee by articular injection, and followed up for 12 month. Articular cartilage changes will be determined by T2-weighted MRI (Cartigram) at 6 and 12 month. Clinical assessment will measure the pain by the visual analogue scale (VAS), the self-reported functional status by Heath Assessment Questionnaire (HAQ), and the quality of life by Short Form 36 questionnaire (SF-36) at 3, 6 and 12 month. The working hypothesis proposes that the expected regenerative articular cartilage effect of the MSC will be produced to a measurable degree by imaging procedures and clinical questionnaires.

NCT ID: NCT01221441 Completed - Clinical trials for Osteoarthritis, Knee

Study of TG-C in Patients With Grade 3 Degenerative Joint Disease of the Knee

Start date: May 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to see if we can safely regenerate cartilage without invasive surgery using a biologic product called TissueGene-C.

NCT ID: NCT01187316 Completed - Clinical trials for Temporomandibular Joint Disorders

Treatment of Temporomandibular Disorders

Start date: April 2007
Phase: N/A
Study type: Interventional

The aim of the present study was to carry out a pilot project comparing the effectiveness of two therapeutic approaches to temporomandibular disorders (TMDs) in adolescents. Eight female individuals diagnosed based on the Research Diagnosis Criteria for TMDs (RDC/TMD-axis 1)were randomly divided into two groups: 1) Massage therapy and muscle stretching (n=4); and 2) transcutaneous electrical nerve stimulation (TENS) (n=4). Regardless the treatment, ten sessions were held for each patient and two measurements (baseline and 10th session) were performed for the assessment of symptom evolution using a visual analog scale (VAS), maximum opening of the mouth (MOM) and pressure pain threshold (PPT). Statistical analysis wiil be carefully selected.

NCT ID: NCT01145157 Completed - Joint Disease Clinical Trials

A Comparison Between Signature Total Knee Arthroplasty (TKA) to Conventional TKA and Computer Assisted TKA

Start date: July 2010
Phase: N/A
Study type: Interventional

This is a prospective, randomised clinical outcomes study comparing the Signature Personalised Patient Care, Conventional Total Knee Arthroplasty and Computer Assisted Navigation, using Vanguard Knee System. The aim of the study is to evaluate the safety and efficacy of TKA using Signature Personalised Patient Care compared to Conventional TKA and Computer Assisted Navigation.

NCT ID: NCT01121146 Completed - Osteoarthritis Clinical Trials

Study Comparing Marathon Polyethylene and Enduron Polyethylene Acetabular Liners Used in Total Hip Arthroplasty

Start date: December 1998
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether crosslinked Marathon and standard Enduron polyethylene liners show differences in bone loss around the hip implant.

NCT ID: NCT01113177 Completed - Clinical trials for Temporomandibular Joint Disorder

Effect of Functional Treatment on Mandibular Asymmetric Growth

Start date: June 1994
Phase: N/A
Study type: Observational

Temporomandibular joint (TMJ) arthritis is known to alter the mandibular development in children diagnosed with juvenile idiopathic arthritis. In a number of cases a genuine breakdown of cartilage and bone is seen in the affected joint which leads to asymmetric mandibular growth in the affected side. In cases of unilateral TMJ involvements severe mandibular asymmetric mandibular growth deviations are seen. We hypothesize that these growth deviations can be minimized and controlled by the use functional orthodontic appliance therapy.