Curriculum Scott A. Wright, MD, FACC Practice
Center for Medical Weight Loss of East Texas, Medical Director
Cardiovascular Associates of East Texas, P.A., Tyler, Texas
Affiliation Education
University of Texas Medical Branch at Galveston
Bachelor of Science (Major: Bioengineering)
University of Texas Medical Branch at Galveston
University of Texas Medical Branch at Galveston
Board Certification
American Board of Internal Medicine – Cardiovascular Disease
Licensure
Nuclear Radiation Certification State of Texas #L04800
Texas State Board of Medical Examiners #K9950
Hospital Appointments
East Texas Medical Center, Tyler, Texas East Texas medical Center, Athens, Texas East Texas Medical Center, Carthage, Texas East Texas Medical Center, Jacksonville, Texas Trinity Mother Frances Hospital, Tyler, Texas Titus Regional Medical Center, Mount Pleasant, Texas Professional Societies/Memberships
Research
Co-Investigator – Paradigm - A multicenter, randomized, double-blind, parallel group, active-controlled study to evaluate the efficacy and safety of LCZ696 compared to enalapril on morbidity and mortality in patients with chronic heart failure and reduced ejection fraction. Co-Investigator - XIENCE™ V: Everolimus Eluting Coronary Stent System (EECSS) USA Post-Approval Study sponsored by Abbott Vascular Inc.
Investigator – MUSIC – Multi-Sensor Monitoring in Congestive Heart Failure Study. Investigator – RECORD AF – REgistry on Cardiac rhythm disORDers: an international, observational, prospective survey assessing the control of Atrial Fibrillation.
Co-Investigator – RE-LY - Randomized Evaluation of Long term anticoagulant therapy (RE-LY) comparing the efficacy and safety of two blinded doses of dabigatran etexilate with open label warfarin for the prevention of stroke and systemic embolism in patients with non-valvular atrial fibrillation: prospective, multi-centre, parallel-group, non-inferiority trial. Co-Investigator – ENDEAVOR IV – A Randomized, Controlled Trial of the Medtronic Endeavor Drug Eluting Coronary Stent System versus the Taxus Paclitaxel-Eluting Coronary Stent System in De Novo Native Coronary Artery Lesions. Co-Investigator – A-HeFT - A Placebo-Controlled Trial of Bidil Added to Standard Therapy In African- American Patients with Heart Failure. Co-Investigator - ACCOMPLISH- A prospective, multicenter, double-blind, randomized, active-controlled trial to compare the effects of Lotrel (amlodipine/benazepril to benazepril and hydrochlorothiazide combined on the reduction of cardiovascular morbidity and mortality in patients with high risk hypertension. Co-Investigator - AMIHOT II – A prospective, Multi-center, randomized study of Aqueous Oxygen Therapy for 90 minutes in Anterior Acute MI patients with successful PCI/stenting presenting within 6 hours from time of symptom onset until time of reperfusion. Co-Investigator – TIMI38/TRITON – A Comparison of CS-747 and Clopidrogrel in Acute Coronary Syndrome Patients who are to Undergo Percutaneous Coronary Intervention; a Phase III, multicenter, randomized, parallel-group, double-dummy, active controlled trial in patients with acute coronary syndrome (ACS), who are to undergo percutaneous coronary intervention (PCI). Co-Investigator – VISION 305 Study - “Vasodilator Induced Stress In Concordance with Adenosine” A multicenter, risk-stratified, randomized, double-blind, double-dummy study drug administration, active- controlled, complete two-arm crossover study with a reference third arm. Co-Investigator - APEX-AMI Study - “A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo- Control ed Study of Pexelizumab in Patients with Acute Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention.” (Assessment of PEXelizumab in Acute Myocardial Infarction)-APEX- AMI. Co-Investigator - XIENCE™ V: Everolimus Eluting Coronary Stent System (EECSS) USA Post-Approval Study sponsored by Abbott Vascular Inc.
High Frequency Electrocardiograms versus Standard Electrocardiograms in Acute Coronary Syndromes: assessing improved sensitivity of HF-EKG in multiple clinical scenarios including adenosine stress testing, percutaneous interventions, risk stratification in emergency departments. Study done in conjunction with NASA. Retrospective Analysis of Adenosine Perfusion Studies in Prediction of Coronary Artery Disease: Comparing results of adenosine perfusion studies with documented coronary anatomy by cardiac catheterization. Masters Thesis, Roger S. Walker, Ph.D. University of Texas at Arlington, Department of Computer Science Developed high resolution laser measurement system for Texas Highway Department
Graduate Research Assistant, Roger S. Walker, Ph.D. University of Texas at Arlington, Department of Computer Science Studied feasibility and software modeling of laser systems. Co-Investigator – SYNERGY - A Prospective, Randomized, Open-Label, Multicenter Study in Patients Presenting with Acute Coronary Syndromes Aventix Pharmaceuticals Protocol Number ENO.GMA.301. IND# 31532
Co-Investigator – A Double-Blind Comparison Of The Incidence Of Hypotension With Two Formulations
Of Intravenous Amiodarone: Cordarone・ I.V. vs Amiodarone Aqueous I.V. Injection - Protocol No.
058K1-312-US Co-Investigator – Otsuka Protocol 21-98-214-01 CASTLE “ A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Parallel-Arm, Study to Assess The Long-Term Effects of Pletal® (Cilostazol) Versus Placebo Administered Orally to Patients with Intermittent Claudication Secondary to Peripheral Arterial Disease Co-Investigator – AMIHOT – TherOx Aqueous Oxygen System – Acute Myocardial Infarction with Hyperoxemic Therapy “AMIHOT” Phase II clinical trial. A Randomized, Controlled, Multicenter Trial of Aqueous Oxygen Infusion for 90 Minutes Post-Primary PTCA/Stent Intervention in Acute Myocardial Infarction Patients. Co-Investigator – A Multicenter, Randomized, Double-blind, Placebo Controlled Study to Evaluate the Efficacy and Safety of Ad5FGF-4 in Patients with Stable Angina. Co-Investigator – Extra Point. Protocol # S1710202. Cardiovascular Safety Study of Nicotine Transdermal System
TRIMIDINETM POWDER Australia: FOR THE TREATMENT OF INFECTIONS DUE TO ORGANISMS SUSCEPTIBLE TO THE COMBINATION OF SULFADIMIDINE AND TRIMETHOPRIM IN HORSES, CALVES, PIGS AND POULTRY. New Zealand: FOR THE TREATMENT OF INFECTIONS DUE TO ORGANISMS SUSCEPTIBLE TO THE COMBINATION OF SULFADIMIDINE AND TRIMETHOPRIM IN HORSES. PRESENTATION: Powder. ACTIVE CONSTITUENTS: Each gra
Permission for Medical Treatment This notarized form must be on file Full Name of Band Member: ______________________________________________________ Birth Date: ______________________________________ To Whom It May Concern : I, the undersigned, being the parent, legal guardian, or legal next-of-kin of the band member whose name appears on this form, do hereby authorize any necessary m