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  • A Multi-Center, Open-Label, Extension Study To Evaluate The Long-Term Safety, Efficacy, and Durability Of EN3835 In The Treatment and Retreatment Of Plantar Fibromatosis

    Position: Investigator
    February 2022 – Present
    Sponsor: Endo Pharmaceuticals

  • A Phase 2, Double-Blind, Randomized, Placebo-Controlled Study To Assess The Efficacy, Safety, And Tolerability Of EN3835 Vs Placebo In The Treatment Of Plantar Fibromatosis

    Position: Investigator
    December 2021 – Present
    Sponsor: Endo Pharmaceuticals

  • An Observational, Double-Blind (Sponsor Open), Long-Term Study to Evaluate the Safety and Durability (Efficacy) of Response to EN3835 Compared to Placebo in the Treatment of Adhesive Capsulitis of the Shoulder (Frozen Shoulder)

    Position: Investigator
    March 2021- Present
    Sponsor: Endo Pharmaceuticals

  • A Phase 2, Randomized, Double-Blind, Placebo-Controlled study of the safety and efficacy of EN3835 for the treatment of Adhesive Capsulitis of the shoulder

    Position: Investigator
    October 2020 – Present
    Sponsor: Endo Pharmaceuticals

  • A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of FX006 in Patients with Glenohumeral Osteoarthritis or Shoulder Adhesive Capsulitis

    Position: Investigator
    December 2019 – June 2020
    Sponsor: Flexion Therapeutics

  • A prospective multi-center study comparing REGENETEN in lieu of standard arthroscopic repair of high-grade (>50%) partial-thickness tears.

    Position: Investigator
    December 2018- Present
    Sponsor: Smith & Nephew, Inc

  • Pivotal, Non-Randomized, Historically Controlled, Prospective, Multi-Center Clinical Study of the Easytech Reversed Shoulder System

    Position: Investigator
    November 2018 – Present
    Sponsor: FX Shoulder

  • Post-Market Evaluation of the Rotation Medical Rotator Cuff System

    Position: Investigator
    July 2017- January 2021
    Sponsor: Rotation Medical, Inc./Smith & Nephew

  • A Randomized, Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of XXXXXXXX for the Treatment of Adhesive Capsulitis of the Shoulder.

    Position: Investigator
    March 2014 – March 2015
    Sponsor: Auxilium Pharmaceuticals, Inc.

  • A Multicenter, Double-blind, Double-dummy, Randomized, Parallel Group, Stratified Study to Evaluate the Efficacy and Safety of a Single IV Dose of XXXXXXXX Compared to a Single IV dose of Ondansetron to prevent Postoperative Nausea and Vomiting in Pediatric Patients.

    Position: Investigator
    June 2011- October 2012
    Sponsor: Helsinn Healthcare

  • A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Assess the Efficacy and Safety of XXXXXXX Patches in Adolescent Subjects with Ankle Sprain

    Position: Investigator
    May 2010 – March 2011
    Sponsor: Hisamitsu Pharmaceutical Co.

  • A Prospective Study to Evaluate Surgical Outcomes in Subjects With Full-Thickness Rotator Cuff Tears Treated by Means of a Double-Row Arthroscopic Repair.

    Position: Investigator
    February 2009 – September 2011
    Sponsor: Wyeth

  • A multicenter, randomized, double-blind, placebo-controlled trial of three injections of SUPARTZ (sodium hyaluronate) for the treatment of chronic shoulder pain associated with glenohumeral osteoarthritis.

    Position: Investigator
    December 2007 – September 2009
    Sponsor: Smith & Nephew, Inc

  • Regulation of Coagulation in Orthopedic Surgery to Prevent DVT and PE; a controlled, double-blind, randomized study of XXXXXXX in the prevention of VTE in subjects undergoing elective total knee replacement

    Position: Sub Investigator
    March 2007 – February 2008
    Sponsor: Bayer

  • Regulation of Coagulation in Orthopedic Surgery to Prevent DVT and PE, controlled, double-blind, randomized study of XXXXX in the extended prevention of VTE in patients undergoing elective total hip replacement

    Position: Sub Investigator
    July 2006 – March 2007
    Sponsor: Bayer

  • Stemless reverse shoulder arthroplasty: clinical and radiologic outcomes with minimum 2 years' follow-up

    Recently, a stemless reverse shoulder arthroplasty (RSA) design was developed to preserve bone stock. Clinical and radiologic studies of this design in larger cohorts with >100 patients are not frequent. The purpose of this study was to present the clinical and radiologic results of a newly developed stemless RSA implant.

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  • Increased stiffness and reoperation rate in partial rotator cuff repairs treated with a bovine patch

    a propensity-matched trial

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  • Two-year outcomes with a bioinductive collagen implant used in augmentation of arthroscopic repair of full-thickness rotator cuff tears: final results of a prospective multicenter study

    Full-thickness rotator cuff tears (FTRCTs) represent a common shoulder injury that, if untreated, can progress in size, become increasingly painful, and inhibit function. These lesions are often surgically repaired, with double-row arthroscopic repair often preferred for larger tears.

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  • Specific Design of a Press Fit Humeral Stem Provides low Stress Shielding in Reverse Shoulder Arthroplasty at minimum 5 Years FU

    Press fit fixation is becoming more popular in RSA to preserve, in theory, bone capital. Several studies report that bone resorption can be very high around humeral stems depending on their size, shape and mode of fixation.

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  • Failure analysis of rotator cuff repair: a comparison of three double-row techniques

    The use of suture anchors has made arthroscopic repair of the torn rotator cuff possible. However, objective evaluations have demonstrated high failure rates. The goal of this study was to compare the modes and rates of failure of two double-row arthroscopic repair techniques and the mini-open double-row technique.

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  • Intramedullary nailing of humeral shaft fractures with a locking flexible nail

    Studies on intramedullary nailing of humeral shaft fractures in the orthopaedic literature have shown mixed results. The purpose of this investigation was to document the clinical outcome and complications associated with the use of a new flexible, locking intramedullary nail that can be implanted in the humerus in either a retrograde or an antegrade manner without violating the rotator cuff mechanism or damaging the articular surface of the humeral head.

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  • Functional outcome of patients with femoral head fractures associated with hip dislocations

    Fracture of the femoral head after hip dislocation is a relatively rare injury often associated with a poor functional outcome. Twenty-six patients who sustained femoral head fractures were evaluated using radiographs, clinical examinations, and a validated outcome scoring system.

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