Cervical Artificial disc: Kineflex C
SI Joint Pain

Clinical Trials

Principal Investigator
Fabien Bitan, M.D.

Lenox Hill Hospital

Study Coordinator
Tom Ross
Phone: 212 744-8114 ext 238

Clinical Trial Subjects' Responsibilities:

  • Subjects must read, understand and sign the Informed Consent and Research Authorization Forms
  • Subjects must meet all of the specific study inclusion/exclusion criteria
  • Subjects must undergo all appropriate preoperative requirements
  • Subjects must be willing to undergo surgical treatment
  • Subjects must be available for examinations and x-rays at the following intervals:
    • Postop
    • 6-Week
    • 3-Month
    • 6-Month
    • 1-Year
    • 2-Year

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