A Randomized, Single-Blind, Active-Controlled, Dose-Ranging Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of Local Administration of DepoTXA for Reduced Postsurgical Bleeding in Subjects Undergoing Total Knee Arthroplasty Save

Date Added
December 13th, 2016
PRO Number
Pro00060470
Researcher
Richard Friedman
Keywords
Surgery
Summary

The study is to see how safe and effective a drug called Liposomal tranexamic acid (DepoTXA) is in reducing postsurgical bleeding compared with intravenous (IV ? into a vein) Tranexamic Acid (TXA) in people undergoing total knee arthroplasty (TKA), otherwise known as knee replacement surgery. The study is an eight week study with a total of four visits with two of them follow-up telephone calls.

Institution
MUSC
Recruitment Contact
Lisa Mock
843-876-2211
mockl@musc.edu

An Open Label, Multi-Center, Retrospective and Prospective Evaluation of Shoulder Arthroplasty Clinical and Radiographic Outcomes Save

Date Added
February 18th, 2014
PRO Number
Pro00030914
Researcher
Richard Friedman
Keywords
Joint, Pain, Surgery
Summary

The purpose of this study is to collect and evaluate clinical and radiographic outcomes data on patients who have undergone, or will undergo, shoulder replacement surgery. Patients who receive a device from the Equinoxe® Shoulder System, manufactured and distributed by Exactech, Inc as well as patients who receive a device from another shoulder arthroplasty system may be included in this study.

Institution
MUSC
Recruitment Contact
Lisa Mock
843-876-2211
mockl@musc.edu

A Post-Market Domestic (US) and International Data Collection to Assess Hip Replacement Systems Manufactured and/or Distributed by Exactech. Save

Date Added
February 18th, 2014
PRO Number
Pro00030758
Researcher
Richard Friedman
Keywords
Joint, Pain, Surgery
Summary

To collect data to further affirm the safety and effectiveness of the hip replacement systems manufactured and/or dustrubuted by Exactech, Inc. Data will be collected in order to provide post-market subjective and objective evidence of safety and effectivenss. Data may be analyzed to support future presentation and publication of theses systems and will be made available in the event Exactech is required to provide clinical evidence of the post market outcomes of the devices.

Institution
MUSC
Recruitment Contact
Lisa Mock
843-876-2211
mockl@musc.edu

A Post-Market Domestic (US) and International Data Collection to Assess the Optetrak® Knee Stystem. Save

Date Added
February 18th, 2014
PRO Number
Pro00030785
Researcher
Richard Friedman
Keywords
Joint, Pain, Surgery
Summary

The study will collect data to further affirm the safety and effectiveness of the Optetrak® Knee System product lines. Data will be collected in order to provide post-market subjective and objective evidednce of safety and effectivness. Data may be analyzed to support future presentation and publication of the Optetrak® Knee Systems and will be made available in the event Exactech is required to provide clinical evidence of the post market outcomes of the Optetrak Knee devices.

Institution
MUSC
Recruitment Contact
Lisa Mock
843-876-2211
mockl@musc.edu

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