Surgical Treatment Comparison for Recurrent Lumbar Disc Herniation

NCT00444405 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2020-02-27

No results posted yet for this study

Summary

The purpose of this study is to compare patients who underwent decompression/discectomy with pedicle screw fusion to patients who received decompression/discectomy without fusion.

Conditions

  • Low Back Pain
  • Recurrent Lumbar Disc Herniation

Sponsors & Collaborators

  • Mercy Research

    lead OTHER

Principal Investigators

  • Alan M. Scarrow, MD, JD · St. John's Health System, Missouri

Eligibility

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

Timeline & Regulatory

Start
2007-03-31
Primary Completion
2009-04-30
Completion
2009-04-30

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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 NCT00444405 on ClinicalTrials.gov