Clinical Trials
Principal Investigator
Fabien Bitan, M.D.
Co-Investigator
Iris Yaron, M.D.
Institution
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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