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Osteoarthritis clinical trials

View clinical trials related to Osteoarthritis.

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NCT ID: NCT01326156 Active, not recruiting - Clinical trials for Osteoarthritis, Knee

Study of Knee Replacements for Patellofemoral Osteoarthritis

PFA/TKR
Start date: June 2007
Phase: N/A
Study type: Interventional

This is a randomized comparison of PFA and TKR in treatment of isolated patellofemoral osteoarthritis.

NCT ID: NCT01319227 Active, not recruiting - Osteoarthritis Clinical Trials

Periprosthetic Bone Remodeling Around Uncemented Components in Total Hip Arthroplasty

PeriBRUSBRAC
Start date: October 2009
Phase: N/A
Study type: Interventional

This is a randomized clinical trial comparing two different uncemented femoral stems and two different uncemented sockets using Dual-energy x-ray absorptiometry, Radiostereometry and clinical evaluation. Hypothesis: 1. A short uncemented stem gives less periprosthetic bone resorption in the proximal femur than a conventional uncemented stem. 2. An uncemented acetabular component with a backside of three-dimensional Titanium porous construct gives less periprosthetic bone resorption than a backside covered with a conventional porous coating with Titanium-beads and a hydroxy-apatite layer.

NCT ID: NCT01307384 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

Zimmer Continuum Metal on Polyethylene (MoP) PostMarket Clinical Followup (PMCF) Study

Start date: March 29, 2011
Phase:
Study type: Observational

This is a prospective, multi-center, non-randomized, non-controlled study designed to obtain survival and outcome data on the Continuum Metal on Polyethylene Acetabular System when used in primary total hip arthroplasty.

NCT ID: NCT01288066 Active, not recruiting - Osteoarthritis Clinical Trials

Effectiveness of Hemi- Versus Total Shoulder Arthroplasty Using Implants of the "Epoca" System

Epoca H vs T
Start date: September 2011
Phase: N/A
Study type: Interventional

The clinical question on whether or not to replace the glenoid component in patients with a degenerative shoulder disease, has not been answered yet in a randomized study with enough statistical power. In this study, patients are randomly allocated to a treatment with a hemi- or total shoulder arthroplasty using implants of the Epoca system. The primary objective is the comparison of pain and function between the treatment groups after 5 years using the Constant score.

NCT ID: NCT01258985 Active, not recruiting - Knee Osteoarthritis Clinical Trials

Tai Chi and Physical Therapy for Knee Osteoarthritis

TCPT
Start date: March 2011
Phase: N/A
Study type: Interventional

We will conduct a large randomized controlled trial comparing the effectiveness and cost-effectiveness of Tai Chi mind-body exercise and standard-of-care Physical Therapy for Knee Osteoarthritis.

NCT ID: NCT01194817 Active, not recruiting - Knee Osteoarthritis Clinical Trials

A Prospective, Randomized Study Comparing Cemented and Cementless Total Knee Replacement

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

The purpose of this study is to compare the the Nexgen knee replacement system using cementless fixation with the same system using cemented fixation. At minimum 2-year follow-up, the hypothesis is that NexGen total knee arthroplasties using cementless and cemented fixation will demonstrate no differences in clinical outcome based on Oxford and Knee Society scores, patient-assessed visual analog pain, clinical complications, radiographic fixation and implant survivorship.

NCT ID: NCT01113762 Active, not recruiting - Osteoarthritis, Hip Clinical Trials

Metal-metal Articulations Versus Standard 28 mm Cementless Total Hip Arthroplasty

Start date: February 2007
Phase: Phase 2
Study type: Interventional

Younger hip patients often need revision of their hip replacement due to wear and loosening. Newer concepts (resurfacing and large head total hip replacement) with articulation surfaces in metal may reduce the wear, increase the longevity of the implant and give an improved function. The possible downside is that these concepts releases metal debris to the body. The investigators wish to see if the newer interventions are a clinical improvement compared to standard. The investigators also wish to investigate the extent of metal released to the body and any effect on the immune system. Finally the investigators wish to investigate the stability of these new implants and their ability to preserve the bone around the implant. The investigators hypothesis is: That the metal on metal articulations will not have better clinical outcomes than standard The resurfacing implant is expected to preserve the bone of the upper femoral bone. The implants are expected to be stabile within the first year.

NCT ID: NCT01107340 Active, not recruiting - Osteoarthritis Clinical Trials

AMIStem Primary Hip System Prospective Post-marketing Multi-centre Surveillance Study

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

This is a multicentre post-marketing prospective study to evaluate performance and clinical outcomes of AMIIStem primary hip system.

NCT ID: NCT01099371 Active, not recruiting - Knee Osteoarthritis Clinical Trials

Resistance Training in Knee Osteoarthritis

Start date: February 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether: 1. Progressive resistance training improves pain and disability 2. Progressive Resistance training improves muscular strength, ability to walk and quality of life

NCT ID: NCT01079390 Active, not recruiting - Clinical trials for Osteoarthritis, Knee

An Acupuncture Functional Magnetic Resonance Imaging (fMRI) Study on Chronic Pain: Response Reliability and Dose Effect

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

In this proposal, we plan to dynamically investigate brain response to verum acupuncture (of two different "doses") and placebo acupuncture, using a paradigm that approximates clinical acupuncture practice across multiple treatment sessions in knee osteoarthritis (OA) patients. This proposal aims to: 1) characterize session-to-session brain responses to verum / sham acupuncture treatment (reliability of response) for OA patients, and 2) investigate how different "doses" of acupuncture influence brain response and acupuncture efficacy (impact of dose). The findings of this project will deepen our biological understanding on why and how acupuncture can treat chronic pain and what happens in the brain during the multiple-session acupuncture treatment.