Status:
TERMINATED
Study of Low Back Pain Using CERSR® Imaging Technology
Lead Sponsor:
Verium Diagnostics, Inc.
Conditions:
Low Back Pain
Eligibility:
All Genders
18-70 years
Brief Summary
The purpose of this research study is to measure with CERSR® (Computerized Electrophysiological Reconstruction of the Spinal Regions) the electrical signals made by the muscles in the lower back 1) wh...
Detailed Description
The purpose of this research study is to measure with CERSR® (Computerized Electrophysiological Reconstruction of the Spinal Regions) the electrical signals made by the muscles in the lower back 1) wh...
Eligibility Criteria
Inclusion
- Inclusion Criteria Groups A, B and C:
- Male and female employees of the study center.
- Between the ages of 18 and 70 years.
- Current employees as well as new hires.
- Exclusion Criteria Group A:
- 1\. Low back pain.
- Exclusion Criteria Group B:
- Low back pain due to fracture, tumor, infection, cauda equina, severe neurological deficit.
- Pregnant.
- Sensitivity to isopropyl alcohol used to prepare the low back surface.
- Inability to complete the required collection positions for the CERSR® scan.
- Inability or unwillingness to adhere to the protocol and follow-up schedule.
- Anyone under care of a physician for active liability or workman compensation cases.
- Anyone who has had an open spinal procedure in the last three months.
- Anyone who has undergone spine injections within the last two months.
- Exclusion Criteria Group C:
- Low back pain due to fracture, tumor, infection, cauda equina, severe neurological deficit
- Pregnant.
- Sensitivity to isopropyl alcohol used to prepare the low back surface.
- Inability to complete the required collection positions for the CERSR scan.
- Inability or unwillingness to adhere to the protocol and follow-up schedule.
- Anyone under care of a physician for active liability or workman compensation cases.
- Anyone who has had an open spinal procedure in the last three months.
- Anyone who has undergone spine injections within the last two months.
- Anyone who is currently undergoing physical therapy or chiropractic treatments.
Exclusion
Key Trial Info
Start Date :
May 1 2011
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
Estimated Enrollment :
290 Patients enrolled
Trial Details
Trial ID
NCT01401660
Start Date
May 1 2011
Last Update
August 1 2011
Active Locations (2)
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1
Summa Center for Clinical Trials
Akron, Ohio, United States, 44304-1619
2
Summa St. Thomas Hospital
Akron, Ohio, United States, 44310-3110