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Post-traumatic; Arthrosis clinical trials

View clinical trials related to Post-traumatic; Arthrosis.

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NCT ID: NCT04875156 Completed - Clinical trials for Osteoarthritis Thumb

The Angle of the Metacarpophalangeal Joint of the Thumb During Maximal Pinch Strength

Start date: September 23, 2020
Phase: N/A
Study type: Interventional

The aim of the study is to measure the position of the metacarpophalangeal joint of the thumb during key-pinch, tripod-pinch and opposition-pinch in normal volunteers, to determine the optimal position of metacarpophalangeal joint arthrodesis.

NCT ID: NCT04079127 Completed - Clinical trials for Rheumatoid Arthritis

Avenir Müller Hip Stem Post Market Surveillance Study

Start date: January 9, 2010
Phase:
Study type: Observational

This study is a Post Market Clinical Follow up study to fulfil the post market surveillance obligations according to Medical Device Directive and European Medical Device Vigilance System (MEDDEV) 2.12-2. The data collected from this study will serve the purpose of confirming safety and performance of the Avenir Müller Hip Stem.

NCT ID: NCT03681639 Completed - Clinical trials for Rheumatoid Arthritis

Metasul Monoblock Component™ Cup in a Hip Resurfacing Application With the Durom® Hip Resurfacing Femoral Component

Start date: August 1, 2009
Phase: N/A
Study type: Interventional

The Zimmer Hip Resurfacing System Post-Market Clinical Follow-up study will examine the safety and efficacy of this device in the young and/or active patient with advanced hip disease.

NCT ID: NCT03382652 Completed - Osteoarthritis Clinical Trials

Continuum™ Metal Bearing System in Total Hip Arthroplasty

Start date: February 9, 2011
Phase:
Study type: Observational

The study is a multi-center, prospective, non-controlled, consecutive cohort post market surveillance study. The objective of this study is to obtain survival and outcome data on the Continuum Metal Bearing System in primary total hip arthroplasty.

NCT ID: NCT03111407 Completed - Knee Osteoarthritis Clinical Trials

iAssist vs. Conventional Instrumentation in Total Knee Arthroplasty

Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this prospective study is to evaluate Zimmer® iASSIST™ with respect to radiographic, clinical and economic outcomes and compared to conventional instrumentation in primary total knee arthroplasty (NexGen or Persona knee implants).

NCT ID: NCT02756702 Completed - Clinical trials for Rheumatoid Arthritis

All Polyethylene Tibia-VEGA Kiel

APT-VEGA_KI
Start date: March 2016
Phase:
Study type: Observational

Obligatory Post-Marketing Clinical Follow-up (PMCF) as part of the post marketing surveillance plan for the product under investigation For this PMCF only CE-marked medical devices will be used within their intended purpose and no additional invasive or other stressful examinations are to be carried out (acc. to MPG §23b).

NCT ID: NCT02399046 Completed - Osteoarthritis Clinical Trials

A Clinical Trial Study of Knee System in Primary Total Knee Arthroplasty in China

Start date: August 17, 2017
Phase: N/A
Study type: Interventional

A clinical trial of total knee system used in Primary Total Knee Arthroplasty in China.

NCT ID: NCT01413061 Completed - Clinical trials for Post-traumatic; Arthrosis

Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft

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

The purpose of this clinical trial is to evaluate the outcome of implanting AlloStem® graft with appropriate rigid internal fixation hardware as an alternative to autograft bone graft with rigid fixation in subtalar arthrodesis procedures. The primary objective of this clinical trial is to compare the overall fusion rate of the investigational to the control treatment. Fusion will be determined by clinical findings, radiographs and computed tomography (CT) of the subtalar joint 24 weeks (6 months) after the trial surgery.

NCT ID: NCT00822640 Completed - Clinical trials for Rheumatoid Arthritis

Comparison of Rotating vs. Fixed Platform of the COLUMBUS Knee Prosthesis

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

A population of 100 patients randomised to rotating and fixed PE inlays in the Columbus knee prosthesis received a navigated TKR. Knee Society Score as primary endpoint, Oxford Score, and postoperative ROM after one year will be compared.

NCT ID: NCT00492973 Completed - Osteoarthritis Clinical Trials

Do Corticosteroid Injections During Total Knee Replacement Improve Early Clinical Results?

Start date: March 2006
Phase: N/A
Study type: Interventional

Prior to surgery, a pharmacist will randomly assign participating patients to one of two groups. One group will get an injection in the knee during surgery that contains medications to limit pain and an antibiotic. A second group will get an injection in the knee during surgery that contains the same pain medications and antibiotic along with a corticosteroid to control inflammation. Corticosteroids are anti-inflammatory medications, not to be confused with muscle-building anabolic steroids you may have heard about in the news. Each patient will have an equal chance of being in either of the two groups. This study will test the safety and efficacy of methylprednisolone acetate in the treatment of pain and inflammation following total knee replacement.