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Osteoarthritis clinical trials

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NCT ID: NCT00988468 Terminated - Knee Osteoarthritis Clinical Trials

Manual Therapy Versus Exercise on Knee Osteoarthritis

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

Earlier research has shown that exercising while receiving manual therapy improves function and reduces pain in people with knee osteoarthritis. However, very little is known about the mechanisms by which manual therapy and exercise reduce pain and improve function. This study will ask subjects with knee osteoarthritis to receive one of the following interventions: (1) no treatment, (2) exercise only, or (3) manual therapy only. Measures will be taken of the patient's knee range of motion, knee swelling and pain before and after receiving the intervention. These measures will be analyzed to determine what effect exercise and manual therapy applied to the knee have on improving knee range of motion and reducing knee pain and swelling. Swelling will be measured using an ultrasound device which is used to take pictures inside the knee. This type of ultrasound measurement is painless and harmless.

NCT ID: NCT00985621 Terminated - Osteoarthritis Clinical Trials

Tanezumab In Osteoarthritis Of The Hip Or Knee

Start date: October 30, 2009
Phase: Phase 3
Study type: Interventional

The purpose of the study is to test the efficacy and safety of 2 doses of tanezumab compared to oxycodone CR and placebo in patients with osteoarthritis

NCT ID: NCT00983762 Terminated - Knee Osteoarthritis Clinical Trials

Comparison of Functional Outcomes of Three Surgical Approaches in Knee Arthroplasty

Start date: June 2009
Phase: N/A
Study type: Observational

A functional outcomes comparison study of three surgical techniques using minimally invasive surgery mini-incision (MIS) for total knee arthroplasty (TKA), standard para-patellar TKA and the unicompartmental knee arthroplasty performed over a 2+ year post-op period.

NCT ID: NCT00982280 Terminated - Chronic Pain Clinical Trials

Evaluation of Effectiveness and Tolerability of Tapentadol Hydrochloride in Subjects With Severe Pain Due to Osteoarthritis Taking WHO Step III Analgesics But Showing a Lack of Tolerability.

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The main objective of the study is to evaluate the effectiveness, tolerability, and safety of tapentadol hydrochloride prolonged release (PR) in participants suffering from severe chronic pain due to osteoarthritis of the knee who are taking WHO Step III analgesics and show lack of tolerability. This is a clinical effectiveness trial designed to establish a link between anticipated clinical outcomes and the clinical practice by means of selected measures of clinical and subject-reported outcome. The trial will compare the effectiveness of previous analgesic treatment (WHO Step III) with that of tapentadol hydrochloride PR treatment during defined periods of evaluation.

NCT ID: NCT00973141 Terminated - Pain Clinical Trials

A Dose-ranging Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Osteoarthritis-related Pain

Start date: September 16, 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the safety and effectiveness of different doses of JNJ-42160443 with placebo in the treatment of chronic, moderate to severe knee or hip pain in patients with a diagnosis of osteoarthritis.

NCT ID: NCT00960804 Terminated - Osteoarthritis Clinical Trials

Long-Term Study Of The Safety Of Tanezumab In Arthritis Patients

Start date: February 15, 2010
Phase: Phase 3
Study type: Interventional

Tanezumab, administered for up to 1 1/2 years, reduces the pain of osteoarthritis without affecting how nerve impulses are transmitted in sensory nerves

NCT ID: NCT00904605 Terminated - Clinical trials for Osteoarthritis of the Knee

Lidocaine Patch Versus Celecoxib in Pain From Osteoarthritis of the Knee

Start date: June 2004
Phase: Phase 4
Study type: Interventional

Patients with unilateral or bilateral osteoarthritis of the knee participated in a Phase IV clinical trial to assess the efficacy of Lidoderm compared with celecoxib 200mg in treating pain from osteoarthritis of the knee.

NCT ID: NCT00878501 Terminated - Pain Clinical Trials

Study to Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetics of AZD1386 in Patients With Osteoarthritis (OA) of the Knee

OA19
Start date: March 2009
Phase: Phase 2
Study type: Interventional

The primary aim of this study is to investigate if AZD1386 is efficacious as an analgesic in patients with osteoarthritis of the knee and at what dose. This will be done by comparing the effect of AZD1386 to placebo ("inactive substance") on pain.

NCT ID: NCT00878046 Terminated - Osteoarthritis Clinical Trials

Multi-centre Study to Assess Long-term Safety and Efficacy of the Silent™ Hip Prosthesis in Primary THR

Start date: May 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the Silent™ hip is effective in the treatment of patients with hip joint disease requiring a total hip replacement. Patients who enter the study will be evaluated at regular intervals following hip surgery using patient, clinical and x-ray assessments. A subset of patients will undergo scans to allow the bone mineral density of the bone surrounding the implant to be monitored

NCT ID: NCT00873444 Terminated - Osteoarthritis Clinical Trials

A Randomised Study to Compare Metal Ion Release and Long-term Performance of the Pinnacle™ Cup With a Ceramic-on-Metal or a Metal-on-Metal Bearing

Start date: July 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to monitor the performance and compare the metal ion release of two bearing combinations, ceramic-on-metal and metal-on-metal in the treatment of patients with hip joint disease requiring a total hip replacement. Patients who enter the study will be randomly allocated to one of the bearing combinations and will be evaluated at regular intervals using, patient, clinical and x-ray assessments. Patients will also have blood samples taken at regular intervals to allow the metal ion levels to be determined.