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Osteoarthritis clinical trials

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NCT ID: NCT03566082 Completed - Clinical trials for Degenerative Joint Disease of Hip

Post-Approval Study of the R3 Biolox Delta Ceramic Acetabular System - Europe

R3 EU PAS
Start date: May 28, 2009
Phase:
Study type: Observational

The purpose of this prospective, multicenter, single arm study is to confirm the long-term safety and effectiveness of the R3 delta Ceramic Acetabular System PMA (P150030) by evaluating long-term (10 years after surgery) follow-up results.

NCT ID: NCT03563690 Completed - Knee Osteoarthritis Clinical Trials

Different Kinds of Acupuncture Treatment for Knee Osteoarthritis

Start date: July 3, 2018
Phase: N/A
Study type: Interventional

Knee osteoarthritis (KOA) a chronic disease with symptoms of persistent pain or rest pain , joint stiffness, numbness, limitation of activity and even disability, with significant associated costs and effects on individuals' life quality. Acupuncture as an approach for the management of chronic pain, is receiving increasing recognition from both the public and professionals. The aim of this study is to indicate the effects of three commonly used acupuncture treatments for KOA.

NCT ID: NCT03561779 Completed - Clinical trials for Osteoarthritis, Knee

Clinical Trial of YYD302 (Phase3) for Treatment of Osteoarthritis of the Knee

Start date: February 21, 2018
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, active-controlled, multi-center, phase 3 study to evaluate the safety and efficacy of intraarticular hyaluronic acid(YYD302) for osteoarthritis of the knee after 12 weeks of treatment and retreatment

NCT ID: NCT03558204 Completed - Clinical trials for Thumb Osteoarthritis

Thumb Carpometacarpal Joint Denervation Versus Trapeziectomy

Start date: August 1, 2018
Phase:
Study type: Observational

This is a prospective study tracking the outcomes of patients who undergo either of two treatments for thumb carpo-metacarpal joint arthritis: trapeziectomy with ligament reconstruction (LRTI) or denervation.

NCT ID: NCT03556787 Completed - Clinical trials for Osteoarthritis, Knee

An Evaluation of a Gender Specific Insole to Provide Relief From Knee Pain Due to Osteoarthritis or General Anterior Knee Pain in Male Subjects When Used in Foot Wear Over a Period of Four Weeks

Start date: June 4, 2018
Phase: N/A
Study type: Interventional

The primary objective of this trial is to demonstrate the ability of a full length foam insole to provide relief from pain due to osteoarthritis of the knee or general knee pain when used in foot wear for a 4-week period of time. The secondary objectives comprise the evaluation of the insole's ability to provide appropriate shoe fit and comfort as well as relief from osteoarthritis/ general knee pain after short-term use. The safety and tolerability of the test articles in terms of adverse events (AE) will also be investigated.

NCT ID: NCT03556423 Completed - Chronic Pain Clinical Trials

Neurophysiological Mechanisms Involved in Knee Osteoarthritis

Start date: July 1, 2018
Phase:
Study type: Observational

Introduction: Total knee arthroplasty (TKA) is an effective intervention to relieve people with osteoarthritis (OA). Nevertheless, 15 to 30% of patients continue to experience severe pain following surgery. Recent data suggest that central nervous system (CNS) changes may play a role in OA pain and possibly explain why some patients have poorer clinical outcomes following TKA. Objectives: Our main objectives are to explore the relationship between OA pain and (1) the integrity of corticospinal system, (2) the efficacy of descending pain inhibition circuits. Methods: Fifty-two patients waiting for TKA will be recruited. The integrity of the corticospinal projections will be measured using transcranial magnetic stimulation (recruitment curve of the affected quadriceps femoris muscle) and the descending pain inhibition circuits (bulbospinal projections) will be assessed by a counter-irritation paradigm (i.e., conditioned pain modulation with immersion of the arm in painfully cold water). Diffuse tension imaging (DTI) will also be used to quantify the strength of these corticospinal and bulbospinal projections. Clinical outcomes will be evaluated before and after arthroplasty with a series of validated questionnaires such as the WOMAC Scale, the McGill Pain Questionnaire and the Brief Pain Inventory. These different neurophysiological and clinical measures will be taken before surgery, 6 months after surgery and 1 year post-surgery. Anticipated results: The investigators expect a moderate association between pain and the strength of the corticospinal and bulbospinal projections. Moreover, it is expected that there will be a moderate association between the strength of the corticospinal/bulbospinal projections and the clinical evolution of patients.

NCT ID: NCT03554720 Completed - Knee Osteoarthritis Clinical Trials

RSA of the ATTUNE Knee System: RCT Comparing Traditional Vs Enhanced-Fixation Device Designs

Start date: July 4, 2018
Phase: N/A
Study type: Interventional

The principal objective of this study is to compare migration patterns between the Attune and Attune S+ PS knee systems using model-based RSA over the first 2 post-operative years. Secondary objectives include; comparison of 2-year migration values against published thresholds for adequate short-term fixation, quantify changes in functional and health status of subjects following surgery and compare between study groups, and assess occurrences of complications following surgery.

NCT ID: NCT03545048 Completed - Knee Osteoarthritis Clinical Trials

Effects of Internet / Web-based Exercises on the Population With Knee Arthritis

Knee OA
Start date: October 15, 2018
Phase: N/A
Study type: Interventional

1. To test whether internet-based exercises reduce the pain in knee OA 2. To check whether internet-based exercises improve the physical activity in the patients with knee OA. 3. To explore the correlation between sleep, knee inflammation (effusion, synovial hypertrophy or/and synovial hyper vascularity) and biomarkers of insulin resistance and knee pain.

NCT ID: NCT03542955 Completed - Clinical trials for Cervical Osteoarthritis

Pulse Shortwave Therapy in Cervical Osteoarthritis

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

The ActiPatch is an FDA cleared pain therapy device that uses pulsed shortwaves to interrupt pain signals at the nerve. 200 patients will be randomized and divided into an ActiPatch treatment group and comparison analgesic drug therapy group . Subjects will be assessed with the Neck Disability Index (NDI) at baseline and at four weeks and VAS scores will be recorded in order to determine the efficacy of the ActiPatch device compared to Etoricoxib. Cervical osteoarthritis causes chronic neck pain which could potentially be alleviated by the ActiPatch without the use of medication.

NCT ID: NCT03542838 Completed - Clinical trials for Osteoarthritis, Knee

Study of Resiniferatoxin for Knee Pain in Moderate to Severe Osteoarthritis

Start date: July 12, 2018
Phase: Phase 1
Study type: Interventional

This study evaluates the safety of resiniferatoxin in patients with moderate to severe knee pain due to osteoarthritis.