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Efficacy Study Image Guided, Auto-Targeted Neurostimulation for the Treatment of Non-Specific Low Back Pain

NCT01132300 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2010-05-28

No results posted yet for this study

Summary

The purpose of this study is:

* Initial evaluation of the clinical effectiveness of Image Guided Transcutaneous Electrical Stimulation (TENS) device for treatment of non-specific low back pain.
* To assess the tolerability and acceptability of the device by the caregiver ("User Friendly").
* To evaluate patients' tolerance by monitoring side effects and tolerability during treatment.

Conditions

  • Low Back Pain

Interventions

DEVICE

Image Guided TENS (Auto-Targeted Neurostimulation, NeMa-st)

Patients will undergo 2 treatments per week during 4 weeks using the device. During the study Patients are allowed to maintain/continue taking medications/ analgesics for pain relief prescribed to them before the study. Medication use will be recorded.

Sponsors & Collaborators

  • Nervomatrix Ltd. Israel

    collaborator UNKNOWN

  • Bnai Zion Medical Center

    lead OTHER_GOV

Principal Investigators

  • Elad Schiff, MD · Bnai Zion Medical Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2010-02-28
Completion
2010-02-28

Countries

  • Israel

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 NCT01132300 on ClinicalTrials.gov