Office Address:
Foot and Ankle Institute
754 South Main, Ste 1
St. George, Utah 84790
Phone: (435) 628-2671

Practice Experience:
  Private Practice: Bellevue, WA 7/93 to 9/95

Education:
  Fellowship:
Virginia Mason, Sports Medicine Center
Dates of Program: 7/92 - 6/93
Podiatric Sports Medicine Fellowship

  Residencies:
CCPM/Ambulatory Surgicenter
Dates of Program: 7/91 - 6/92
Certificate: Podiatric Surgical Residency, (PSR-12)
LA. County/USC Medical Center
Dates of Program: 7/90 - 6/91
Certificate: Rotating Podiatric Residency (RPR)

  Graduate:
California College of Podiatric Medicine
Dates of Attendance: 9/86 - 5/90
Degree: Doctor of Podiatric Medicine

  Undergraduate:
Brigham Young University, Utah
Dates of Attendance: 9/82 - 4/83, 9/84 - 12/85
Degree. B.S. - Microbiology
Dixie College. St. George, Utah
Dates of Attendance: 9/80 - 5/82, 9/83 - 5/84
Degree: Associate of Science


Organizations/Certification:
  Member of American Podiatric Medical Association
  Member of Washington State Podiatric Medical Association
  Board Certified - American Board of Podiatric Surgery

Research Experience:
Foot & Ankle Institute

  Sub Investigator - Multicenter, double-blind, randomized, placebo-control, parallel-group study to evaluate the safety and efficacy of XXXX in patients with neuropathic pain due to diabetic neuropathy.

  Sub Investigator - Clinical Protocol for a Double-Blind, Placebo and Active-Controlled Comparison of the Analgesic Activity of XXXX 40 Mg, Oxycodone 10 Mg/Acetaminophen 1000 Mg (Tylox) and Placebo in Post-Bunionectomy Surgical Patients.

  Sub Investigator - A Double-Blind, Randomized, Controlled Study of the Analgesic Efficacy and Tolerance of Hydrocodone 5 mg/APAP 500 mg, Hydrocodone 10 mg/APAP 1000 mg and Placebo in Patients with Pain Following Bunion Surgery.

  Sub Investigator - A Multi-Center, Double-Blind, Randomized, Parallel Group, Two-Period Study To Evaluate The Efficacy And Safety Of Oral Doses Of An Extended-Release Combination Of XXXX and XXXX, Extended-Release Hydrocodone 15 mg Tablets, Extended-Release Acetaminophen 1000 mg Tablets, And Placebo In The Treatment Of Moderate To Severe Pain In Subjects Undergoing Orthopedic Surgery.

  Sub Investigator - Linezolid IV or PO Compared to Unasyn(IV or Augmentin(Po for the Treatment of Patients with Diabetic Foot Infections-A Randomized, Open Label Phase IV Clinical Trial.

  Sub Investigator - A Multicenter, Double Blind, Double Dummy, Placebo-Controlled Parallel Group Study to Compare the Efficacy, Safety and Tolerability of New Oral Formulation XXXX in Patients with Onychomycosis of the Toenails.

  Sub Investigator - A Multicenter, Randomized, Double Blind, Parallel-Group, Single Dose, Placebo-Controlled, Active Comparator Study of the Efficacy and Safety of XXXX in Subjects Following Bunionectomy Surgery.

  Sub Investigator - A Randomized, Double-Blind, Parallel-Group, Dose-Ranging Multiple-Dose Pilot Study Assessing The Analgesic Efficacy And Safety Of Two- Dose Levels Of XXXX Compared To Intravenous Morphine And Placebo In Patients Following Orthopedic Surgery (Bunionectomy).