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Osteoarthritis, Knee clinical trials

View clinical trials related to Osteoarthritis, Knee.

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NCT ID: NCT00194051 Completed - Obesity Clinical Trials

Symptomatic, Biomechanical and Radiographic Outcomes in Knee Osteoarthritis Following Gastric Bypass Surgery

Start date: February 2003
Phase:
Study type: Observational

Weight is a risk factor for knee osteoarthritis Knee osteoarthritis is associated with abnormal gait biomechanics Gait biomechanics are evaluated in gastric bypass patients before and after losing 100 pounds.

NCT ID: NCT00171691 Completed - Osteoarthritis Clinical Trials

Safety of Diclofenac Sodium Gel in Knee Osteoarthritis

Start date: October 2004
Phase: Phase 3
Study type: Interventional

This study will test the efficacy and safety of topical Voltaren in the treatment of knee osteoarthritis.

NCT ID: NCT00171678 Completed - Osteearthritis Clinical Trials

Efficacy and Safety of Diclofenac Sodium Gel in Knee Osteoarthritis

Start date: October 2004
Phase: Phase 3
Study type: Interventional

This study will test the efficacy and safety of topical diclofenac sodium gel in the treatment of knee osteoarthritis.

NCT ID: NCT00171626 Completed - Osteoarthritis Clinical Trials

Efficacy and Safety of Diclofenac Sodium Gel in Knee Osteoarthritis

Start date: August 2004
Phase: Phase 3
Study type: Interventional

This study will test the efficacy and safety of topical diclofenac sodium gel in the treatment of knee osteoarthritis.

NCT ID: NCT00170872 Completed - Clinical trials for Rheumatoid Arthritis

6 Week Open-label Trial With Lumiracoxib 200mg o.d. in Primary Knee Osteoarthritis or Rheumatoid Arthritis

Start date: November 2004
Phase: Phase 3
Study type: Interventional

This study tested the safety, tolerability and efficacy of lumiracoxib - a COX-2 inhibitor- in patients with primary knee osteoarthritis or rheumatoid arthritis.

NCT ID: NCT00140972 Completed - Osteoarthritis Clinical Trials

A Study to Assess Etoricoxib Versus Diclofenac in Chinese Patients With Osteoarthritis of the Knee or Hip (0663-080)(COMPLETED)

Start date: December 3, 2004
Phase: Phase 4
Study type: Interventional

A Study to Assess Etoricoxib versus Diclofenac in Chinese Patients with Osteoarthritis of the Knee or Hip

NCT ID: NCT00139776 Completed - Clinical trials for Osteoarthritis, Knee

Study Of "Continuous Use" Of Celecoxib Vs. "Usual or Intermittent Use"

Start date: July 2005
Phase: Phase 4
Study type: Interventional

To determine whether "continuous use" of celecoxib over a 6-month period is more efficacious than "usual or intermittent use" in preventing spontaneous osteoarthritis flares of the knee and hip.

NCT ID: NCT00139295 Completed - Clinical trials for Osteoarthritis, Knee

Comparison of Hylastan to Methylprednisolone Acetate in Patients With Symptomatic Osteoarthritis of the Knee

Start date: October 2004
Phase: Phase 3
Study type: Interventional

This is a clinical study to investigate the safety and efficacy of hylastan in treating patients with symptomatic osteoarthritis (OA) of the knee.

NCT ID: NCT00137410 Completed - Osteoarthritis,Knee Clinical Trials

Celebrex Short Versus Long Therapy In Osteoarthritis Of The Knee

Start date: November 2002
Phase: Phase 3
Study type: Interventional

This is a phase III, multicentre, randomized, double blind, parallel-group, pilot study designed to compare a long term (12 weeks) versus a short term (2 weeks) treatment with celecoxib 200 mg/die in treatment and prevention of new flare in patients with osteoarthritis of the knee.

NCT ID: NCT00132587 Completed - Clinical trials for Osteoarthritis, Knee

Total Knee Arthroplasty (TKA) Cemented Versus Cementless

Start date: March 2004
Phase: N/A
Study type: Interventional

The aim of the study is to analyse and to compare the quality of fixation of a femoral implant with or without cement. One hundred thirty patients will be operated on and included with 2 groups, the first one with TKA all cemented and the second one with TKA with a cementless femoral implant. The study criteria include the IKS (International Knee Society) score and the analysis of a radiolucent line at the femur. Patients will be reviewed at 2, 6 and 12 months.