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Total Hip Arthroplasty clinical trials

View clinical trials related to Total Hip Arthroplasty.

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NCT ID: NCT01443975 Completed - Clinical trials for Total Hip Arthroplasty

Clinical Evaluation on the Use of the X-pander Device

X-Pander
Start date: September 2011
Phase: N/A
Study type: Observational

The purpose of this study is to clinically evaluate the use of the x-pander device.

NCT ID: NCT01380665 Withdrawn - Clinical trials for Total Knee Arthroplasty

Prevena™ Incision Management System Over Primarily Closed Hip and Knee Incisions in Patients Immediately Post Total Hip and Knee Arthroplasty

Prevena2009-45
Start date: October 2009
Phase: Phase 4
Study type: Interventional

The intent of this study is to evaluate the Prevena ™ 125 Unit and dressing system, when applied to either the hip or knee area over a surgical cut for the time you are hospitalized.

NCT ID: NCT01312077 Recruiting - Clinical trials for Total Hip Arthroplasty

The Analgesic Efficacy of Periarticular Infiltration of Local Anaesthetic for Total Hip Replacement

Start date: October 2010
Phase: Phase 4
Study type: Interventional

Total hip replacement is a major surgical procedure usually associated with significant pain in the early postoperative period. In our hospital, total hip replacement is routinely performed under spinal anaesthesia with intrathecal bupivacaine local anaesthetic plus opioid in the form of preservative free morphine. The use of 'local infiltration analgesia' as an alternative postoperative analgesic technique has been investigated.In this technique the surgeon infiltrates the surgical site with a long-acting local anaesthetic and places a catheter under direct vision which remains in situ and is used to administer local anaesthetic in the postoperative period until such time as it is removed (when no longer deemed necessary for pain relief or at a pre-set time in the postoperative period e.g. 48 hours). We hypothesize that infiltration of the surgical site with peri- and intraarticular levobupivacaine local anaesthetic would be an efficacious pain management technique and would not be inferior to intrathecal morphine for postoperative pain management.

NCT ID: NCT00896259 Completed - Clinical trials for Total Hip Arthroplasty

Effects of a Late Phase Exercise Program Following Total Hip Arthroplasty

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

A group of orthopedic physiotherapists have developed a late phase program to educate and instruct total hip replacement patients in progressive exercises appropriate for their level of recovery. The components of this program include an educational presentation, individual assessment and exercise prescription. The investigators' intent is to pilot the program using a sample of patients. The objective of this pilot project: To examine the effects of the late phase education session and home-based exercise program in restoring hip muscle strength, gait and function

NCT ID: NCT00883805 Withdrawn - Clinical trials for Total Hip Arthroplasty

Investigation of Systemic Metal Ion Concentration Following a Ceramic-on-metal Total Hip Arthroplasty

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

This is a pilot study to compare systemic concentrations of cobalt and chromium in patients that have previously undergone total hip arthroplasties with ceramic on metal and metal on metal bearing surfaces.

NCT ID: NCT00881998 Completed - Clinical trials for Total Hip Arthroplasty

Study of Two Surgical Approaches for Total Hip Arthroplasty

Start date: n/a
Phase: N/A
Study type: Interventional

A prospective, comparative, randomized single surgeon study comparing minimally invasive total hip arthroplasty (MIS) via anterior approach to conventional total hip arthroplasty via anterolateral transgluteal approach.

NCT ID: NCT00831363 Completed - Clinical trials for Total Hip Arthroplasty

Minimal Invasive Versus Traditional Transgluteal Approach in Total Hip Arthroplasty: a Comparative Gait Analysis

Start date: n/a
Phase: N/A
Study type: Observational

The hypothesis for the present study was that patients receiving a minimally invasive total hip arthroplasty will show a faster improvement on walking ability and mobilization in the immediate postoperative period compared to patients with the standard Hardinge approach. Therefore, the main goal was to evaluate the differences in early rehabilitation of these two different surgical approaches by gait analysis and electromyographical examination as objective methods.

NCT ID: NCT00334165 Completed - Acute Pain Clinical Trials

Auricular Acupuncture for Analgesia During Total Hip Arthroplasty

Start date: June 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The aim is to investigate whether auricular acupuncture is superior to sham acupuncture in relief of acute pain and in reduction of analgesics in patients during total hip arthroplasty