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


Personal Data:
Birthdate: Aug 23, 1953
Place: Littlefield, Arizona
Married: Stephanie Millett Reber
Children: 5

Education:
  High School:
     Virgin Valley High School - Mesquite, Nevada
  Under Graduate:
     -Mesa Community College, Mesa, Arizona
     -Brigham Young University, Provo, Utah
  Post Graduate:
     -California College of Podiatric Medicine, San Francisco, California
     -1 yr. L.A. County Hospital L.A. California
     -1 yr. Residency Training V.A. Hospital, Albuquerque, New Mexico

Organizations/Certification:
  Member of Utah Podiatry Association
  Member of American Podiatric Medical Association
  Board Certified with the American Board of Podiatric Surgery, 1986
  Member of the American College of Foot Surgeons, 1987
  Staff Member:
  Dixie Regional Medical Center
  St. George Surgical Center
  South Main Surgical Center

Civic:
  2000 -- Traveled with Volunteer Medical Team for 2 weeks to Fortaleza, Brazil to perform "club foot" surgery.
  1999 -- Traveled with Volunteer Medical Team for 2 weeks to Fortaleza, Brazil to perform "club foot" surgery.
  1991 -- Traveled with the American Volunteer Medical Team for 3 weeks to Banglidesh to offer medical treatment.
  1985 -- Organized Foot and Ankle Insitute.  Partner, S. Kent Burton D.P.M.

Research Experience:
Foot & Ankle Institute

  Principle 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.

  Principle 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.

  Principle 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.

  Principle 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.

  Principle 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.

  Principle 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).

  Principle 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.