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Arthroplasty, Replacement, Hip clinical trials

View clinical trials related to Arthroplasty, Replacement, Hip.

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NCT ID: NCT01020253 Active, not recruiting - Clinical trials for Arthroplasty, Replacement, Hip

The Effectiveness of Two Osteoporosis Drugs on Prosthetic Bone Mineral Density (BMD) Loss After Total Hip Arthroplasty(THA)

ETOD
Start date: January 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether alendronate and alfacalcidol are effective on prosthetic or lumbar spine BMD after total hip arthroplasty.

NCT ID: NCT00980616 Completed - Clinical trials for Arthroplasty, Replacement, Hip

Use of Local Analgesia With Epinephrine During Total Hip Arthroplasty (THA)

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

The aim is to determine if the use of infiltration with an adrenalin solution in the operative field of Total Hip Arthroplasty (THA), allays a significant reduction of the cumulated volume of bleeding (pre and post operative) without increasing the per and post operative risks. At the same time, the effect on the post operational pains is evaluated.

NCT ID: NCT00962013 Completed - Clinical trials for Arthroplasty, Replacement, Hip

Restoration® Modular Revision Hip System Post Market Study

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

The purpose of this study is to demonstrate survivorship of the femoral stem at 5 years.

NCT ID: NCT00960206 Completed - Clinical trials for Arthroplasty, Replacement, Hip

ABC/Trident® Ceramic Post Approval Study

Start date: March 2003
Phase: N/A
Study type: Interventional

The purpose of the Post Approval Study of the ABC and Trident® systems is to continue to demonstrate the safety and efficacy of the alumina-on-alumina bearing surfaces combined with the appropriate shell in a cementless application.

NCT ID: NCT00958945 Not yet recruiting - Clinical trials for Total Knee Arthroplasty

Retrospective Chart Analysis in the Effective Use of FloSeal in Post-Operative Joint Replacements

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

The purpose of this analysis is to compare Hemoglobin and Hematocrit levels following total hip or knee arthroplasty. The utilization of FloSeal intraoperatively will improve hemostasis postoperatively. Decreasing bleeding time will decrease the drop in level of Hemoglobin and Hematocrit which usually occurs postoperatively.

NCT ID: NCT00958347 Terminated - Clinical trials for Arthroplasty, Replacement, Hip

Omnifit Hydroxylapatite (HA) Hip Outcomes Study

Start date: October 1987
Phase: N/A
Study type: Interventional

The purpose of this study was to obtain up to 25 year post-operative data on the Omnifit Hydroxylapatite (HA) Hip System in support of the hypothesis that it is a satisfactory system for reducing implant loosening, permitting tissue bonding onto the hydroxylapatite surfaces of the implant and providing a safe, efficient, and well-functioning hip in a wide spectrum of clinical circumstances.

NCT ID: NCT00958191 Completed - Clinical trials for Arthroplasty, Replacement, Hip

Trident® X3 Polyethylene Insert Study

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

The primary objective of the study is to demonstrate the linear wear rates of the Trident® X3 polyethylene insert are superior to a polyethylene control group wear rate at 5 years postoperative. This measurement will be evaluated by comparing digitized images of serial radiographs obtained over a follow-up period of 5-years.

NCT ID: NCT00957658 Completed - Clinical trials for Arthroplasty, Replacement, Hip

Accolade® TMZF® Hip Stem Outcomes Study

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

The purpose of this study is to evaluate clinical and radiographic outcome data in patients implanted with the Accolade® TMZF® femoral stem.

NCT ID: NCT00936949 Completed - Clinical trials for Arthroplasty, Replacement, Hip

Posterolateral Surgical Approach Compared With Modified Lateral Approach

Start date: July 2003
Phase: N/A
Study type: Interventional

It has been reported that the operative approaches have an effect on clinical outcome in total hip arthroplasty. The purpose of this prospective study was to compare clinical and radiological outcomes between anterolateral approach and posterolateral approach in total hip arthroplasty.