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Total Joint Arthroplasty clinical trials

View clinical trials related to Total Joint Arthroplasty.

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NCT ID: NCT03673293 Active, not recruiting - Clinical trials for Total Joint Arthroplasty

Measuring Postoperative Mobility, Gait Symmetry and Feedback Following TJA

Start date: May 5, 2018
Phase:
Study type: Observational

The objectives of this study are: 1. The investigators plan to evaluate and validate the use of a novel wireless insole device (Loadsol) that provides real-time biofeedback on post-operative mobility and weight bearing following total joint arthroplasty. 2. The investigators plan to utilize the wireless insole device to determine if biofeedback is sufficient for improving gait symmetry following total joint arthroplasty. 3. The investigators plan to determine if there is a correlation between patient reported outcomes and measured postoperative weight bearing.

NCT ID: NCT03301610 Completed - Pain, Postoperative Clinical Trials

Mobile Educations Effect on Pain Outcomes

Start date: October 23, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to explore the clinical impact of pain management education using a mobile web-based education delivery system compared to standard education delivery. This study seeks to understand the difference between two different education delivery methodologies and the effect on the postoperative pain experience, including participation in treatment plan, knowledge, pain outcomes, and opioid requirements in patients undergoing major hip (THA) and knee (TKA) arthroplasty. It is hypothesized that a real-time, interactive, mobile education system will demonstrate improved pain associated outcomes and higher patient participation when compared to the current standard education delivery method.

NCT ID: NCT01636414 Active, not recruiting - Clinical trials for Total Joint Arthroplasty

Reinfusion Drains vs Tranexamic Acid in Total Joint Arthroplasty

Start date: May 2012
Phase: Phase 4
Study type: Interventional

It is widely reported that a large percentage of total joint replacement patients receive allogeneic (human donor blood) blood transfusions due to perioperative blood loss with numbers ranging from 30% to 80%. The risks of allogenic blood transfusion are well documented in the literature. In addition, they are time-consuming: often lengthening hospital stay and decreasing the availability for postoperative physical therapy. Moreover, they are costly at several hundred dollars per unit, and allogeneic transfusions are linked with immunosuppression and increased postoperative infection rates and wound healing problems, which are devastating complications in this elective, joint replacement population. Several options are available for diminishing the need for allogenic blood transfusion following elective total joint replacement. These include the use of perioperative blood salvage devices (OrthoPAT) and tranexamic acid. While there is data to support the use of both OrthoPat and Tranexamic acid in primary total joint arthroplasty, there is little information comparing one versus the other in terms of efficacy and economics. The purpose of this study is to compare the safety, effectiveness and cost benefit of Hemovac drain, OrthoPAT and Tranexamic Acid to manage blood loss during total hip and total knee replacement surgery.

NCT ID: NCT01577823 Completed - Clinical trials for Total Joint Arthroplasty

Utility of Indwelling Catheter in Orthopaedic Patients Receiving Spinal Anesthesia

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

A study measuring utility of indwelling bladder catheter placement in orthopaedic surgical patients receiving spinal anesthesia. Study will track clinical outcomes, patient satisfaction and cost efficacy. Absence of indwelling bladder catheter may decrease urinary tract infection (UTI) incidence, increase patient satisfaction, and decrease cost burden without increasing postoperative urinary retention (POUR) incidence.