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Intervertebral Disc Augmentation With Minimally Invasive Surgical Procedure

NCT01442922 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1

Last updated 2013-01-17

No results posted yet for this study

Summary

The primary purpose of the study is to establish the degree and duration of pain relief following minimally invasive surgery for a painful degenerative disc.

Conditions

  • Degenerative Disc Disease

Interventions

OTHER

completion of the (VAS) for level of back pain

Patients will complete the (VAS) pre-operatively and post-operatively at 6 wks, and 3, 6, 12, and 24 mos.

OTHER

completion of the (OLBPQ) for assessment of function

Patients will complete the (OLBPQ) pre-operatively and post-operatively at 6 wks, and 3, 6, 12, and 24 mos.

Sponsors & Collaborators

  • University of Florida

    lead OTHER

Principal Investigators

  • Michael Mac Millan, M.D. · University of Florida Department of Orthopaedics and Rehabilitation

Eligibility

Min Age
18 Years
Max Age
44 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2012-12-31
Completion
2012-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01442922 on ClinicalTrials.gov