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Clinical Trial Summary

This trial is designed to preliminary evaluate the efficacy and safety of NIBS system for treatment of chronic low back pain (CLBP) (over 6 months). The trial is of a double blind sham controlled partial crossover design and will involve 2 weekly treatments and evaluations for 6 weeks, with 6 weeks follow-up. The goal of the study is to 1. Asses the CLBP change immediate and long term effect for the trial duration and follow-up. 2. Asses quality of life improvement as measure by sleep quality and questioners. 3. Asses long term neuronal changes or lack thereof in treated and untreated subjects.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02615418
Study type Interventional
Source NIBS NeuroScience Technologies
Contact Iftach Dolev, PhD
Email iftach@nibs.co.il
Status Not yet recruiting
Phase N/A
Start date January 2016
Completion date July 2017

See also
  Status Clinical Trial Phase
Completed NCT02609854 - Sustained Acoustic Medicine for Chronic Low Back Pain Secondary to Herniated Nucleus Pulposus or Other Conditions N/A
Recruiting NCT06453291 - Assessment of Different Clinical Techniques to Treat Patients With Chronic Low Back Pain N/A