The CX-DZ-Ⅱ Intelligent Electroacupuncture Instrument for Neck Pain

Status Completed

Clinical Trial Summary

The present study is a prospective, two-center, randomized, controlled, open-label, non-inferiority trial evaluating the efficacy and safety of a new intelligent electroacupuncture instrument in treating neck pain caused by cervical spondylosis.

Clinical Trial Description

A total of 160 eligible patients will be included in this trial and randomly assigned to experimental group and control group in a 1:1 ratio. In experimental group, selected acupoints will be stimulated by the new intelligent electro-acupuncture instrument; while for control group, electroacupuncture treatment will be accomplished by a pre-existing electro-acupuncture instrument. The duration of treatment will be 2 weeks. The primary outcome is the change of visual analog scale score after one course of treatment. The secondary outcomes are visual analog scale score after each treatment, the responder rate, drug-usage rate of non-steroidal antipyretic analgesics, the occurrence rate of adverse events, defect rate of instrument, and excellent rate of instrument. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03005301
Study type	Interventional
Source	Chengdu University of Traditional Chinese Medicine
Contact
Status	Completed
Phase	N/A
Start date	January 2017
Completion date	June 2018

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