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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01674387
Other study ID # 64385700
Secondary ID ZYSNXD-CCHPGC-JD
Status Completed
Phase N/A
First received
Last updated
Start date August 2012
Est. completion date December 2016

Study information

Verified date August 2021
Source Shanghai University of Traditional Chinese Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose of this test is to observe and objectively evaluate electroacupuncture (EA) therapy on the clinical efficacy in patients with chronic neck pain, and provide a reliable clinical basis for the chronic neck pain treatment and evaluation of efficacy.


Description:

According to statistics, the incidence of chronic neck pain has significantly increased year by year, particularly tending to younger people, as social competition increase fiercely and the pace of people's daily work and life accelerate. Studying the effective treatment and prevention of chronic neck pain has obvious medical, social and economic significance. Purpose of this trial is to observe and objectively evaluate electroacupuncture (EA) therapy on the clinical efficacy in patients with chronic neck pain, and provide a reliable clinical basis for the chronic neck pain treatment and evaluation of efficacy.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 2016
Est. primary completion date August 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. Age of a subject is older than 18 and is younger than 65. 2. With more than 3 months history of neck pain. 3. Informed consent is signed by a subject or his lineal relation. Exclusion Criteria: 1. With serious protopathy or disease ofcardiovascular,liver,renal,gastrointestinal, hematological systems and so on. 2. Psychotic,patients with allergic constitution or easily getting infected or bleeding. 3. Patients have used drugs for preventing neck pain in the last four weeks. 4. Pregnant women or women in lactation.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
acupuncture
56 patients (the EA group) receive the acupuncture treatment at nine acupuncture points: Dazhui (GV14), bilateral Jianzhongshu (SI15), bilateral Jingbailao (EX HN15), bilateral Jiaji (EX-B2) of cervical positive reaction plane (taking two pairs). Besides, bilateral Jianzhongshu (SI15) and bilateral Jiaji (EX-B2) receive the electro acupuncture treatment, with dilatational wave. All the needles retained for 20 minutes, one treatment every other day, 10 times a course, and the treatment assessed after a course.
Other:
comprehensive treatment
Other 56 patients (the matched group) receive the comprehensive treatment, including traction and TENS therapy. Each treatment 20 minutes, one treatment every other day, 10 times a course, and the treatment assessed after a course.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Shanghai University of Traditional Chinese Medicine Longhua Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary chronic neck pain-the Neck Pain Scale (NPQ) 20 days(One course)
Primary the short-form McGill Pain Questionnaire 20 days(One course)
Primary the SF-36 Health Questionnaire combined with Neck Disability Index (NDI). 20 days(one course)
Secondary chronic neck pain-the Neck Pain Scale (NPQ) one month after a course.
Secondary the short-form McGill Pain Questionnaire one month after a course
Secondary the SF-36 Health Questionnaire combined with Neck Disability Index (NDI). one months after a course
See also
  Status Clinical Trial Phase
Completed NCT02033460 - Manual Therapy Versus Manual Therapy and Exercise and Education in Chronic Neck Pain N/A