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Radiofrequency Nerve Ablation Versus Sham to Treat Chronic Low Back Pain Caused by Sacroiliac Joint Dysfunction

NCT01104051 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 28

Last updated 2015-07-29

No results posted yet for this study

Summary

Trial will enroll qualified subjects at a 2:1 ration to receive radiofrequency ablation or sham. At six weeks follow up they will be unblinded; sham subjects will then be given option to receive treatment.

Subjects will be followed after procedure for data collection for economic outcomes and efficacy of treatment.

Conditions

  • Sacroiliac Joint Dysfunction

Sponsors & Collaborators

  • Coastal Orthopedics & Sports Medicine

    lead OTHER

Principal Investigators

  • Richard Bundschu, MD · Coastal Orthopedics

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2015-06-30
Completion
2015-06-30

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 NCT01104051 on ClinicalTrials.gov