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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01250093
Other study ID # Nantou
Secondary ID
Status Completed
Phase N/A
First received November 26, 2010
Last updated November 29, 2010
Start date March 2008
Est. completion date January 2009

Study information

Verified date October 2008
Source China Medical University Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Interventional

Clinical Trial Summary

In order to investigate the therapeutic effect of acupuncture on chronic neck myofacial pain syndrome, the investigaotrs designed a pilot study of a single-blind randomized controlled trial. A total of 34 chronic neck myofacial pain syndrome patients were selected from Department of Neurology of Nantou Hospital, Department of Health. The age ranged from 18 to 85, and all subjects were full informed consent and volunteers. They were divided into two groups of 17 subjects randomly as follows: acupuncture group, acupuncture stainless needles were inserted into bilateral Fenhchi, Jianliao and Houxi acupoints, respectively. The acupuncture needles then were manual twist and de Qi, and remain for 20 min; sham acupuncture group, the methods were identical the acupuncture group, but acupuncture stainless needles were inserted into subcutaneous tissue only. All the subjects were treated with acupuncture two times per week and continuously three weeks, i.e. Six times acupuncture treatment. The therapeutic effect of acupuncture was assessed before and finishing six times acupuncture treatment, and four weeks and twelve weeks after stopping acupuncture, respectively. The index of acupuncture therapeutic effect was according to the range of motion (ROM) of the cervical spine, the intensity of pain (Short-Form McGill Pain Questionnaire; SF-MPQ) and quality of life (SF-36). The investigators expect acupuncture apply to bilateral Fenhchi, Jianliao and Houxi acupoints may relief the pain and motion of chronic neck facial pain syndrome patient, and also improves the life quality.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date January 2009
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- 18-85 year-old patients with neck myofascial pain for more than one month; not received any treatment in the two weeks before participating this study

Exclusion Criteria:

- Fracture or surgery of the cervical spine; Cervical radiculopathy or myelopathy; Any rheumatic disorder; Systemic disorders; Major psychiatric disorder, alcoholism or substance abuse; Coagulation dysfunction, or related medicines; Pregnancy; Contraindications to acupuncture; Refused to sign consent

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Device:
acupuncture


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
China Medical University Hospital