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

Personal Data:
Birthdate: January 12, 1956
Place: Payson, Utah
Married: Lori Ann Chappel
Children: 5

Education:
  Brigham Young University: 1980 - Zoology
  California College of Podiatric Medicine: 1984
  4th year at U.S.C./L.A. county Medical Center
  Residency: Veteran's Administration Medical Center, Albuquerque, New Mexico: 1985.

Board Certification:
  Foot and Ankle Surgery
  American Board of Podiatric Surgery - 1990

Professional Associations:
  American Podiatric Medical Association
  Utah Podiatric Medical Center

Hospital Affiliation:
  Dixie Regional Medical Center: Medical Staff - 1991
  Valley View Medical Center - 1986-1994

Practice:
  Foot and Ankle Institute
  St.George, Utah: in association with Dr. Keith R. Reber

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).