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The Efficacy of the no!no!Back for Chronic Low Back Pain

NCT01620281 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2013-08-06

No results posted yet for this study

Summary

This pilot study is designed to evaluate the efficacy of the no!no!Back continuous passive motion device in relieving of mild to moderate non-specific low back pain.

Conditions

  • Mild to Moderate Chronic Low Back Pain

Interventions

DEVICE

no!no!Back

Self treatments daily for 3 weeks, in up to three 10-minutes sessions

Sponsors & Collaborators

  • Radiancy

    lead INDUSTRY

Principal Investigators

  • Lilach Gavish, PhD · Friedman Skin & Laser Center

  • David J Friedman, MD · Friedman Skin & Laser Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2012-10-31
Completion
2013-02-28

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 NCT01620281 on ClinicalTrials.gov