Spine Clinical Outcomes Research Registry

Full Title of Study

Spine Clinical Outcomes Research Registry (R#06-381)

Purpose of Study

This project involves asking patients to complete quality-of-life questionnaires. Patient responses and information from their medical records will be placed into a research registry that will allow researchers to conduct studies to increase knowledge about spine diseases and disorders, specifically about scoliosis and other spinal deformities.

Basic Inclusion Criteria (requirements for being included in study)

  • Male or female patient of any age
  • Scheduled for surgery for scoliosis, kyphosis, or other spinal deformity

Basic Exclusion Criteria (reasons for being excluded from study)

  • Inability or refusal to provide consent

Study Visit Requirements

Patients are evaluated at 6 weeks, 3 months, 6 months, 12 months and annually thereafter.

Answers to frequently asked questions (FAQs) about clinical trials

For more information about enrolling in this study, please contact Alexandra Lee, alex.lee@nyumc.org or 212-598-6114