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The efficacy of acupotomy combined with muscle activation for patients with myofascial chronic neck pain

The efficacy of acupotomy combined with muscle activation for patients with myofascial chronic neck pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN64518034
Enrollment
30
Registered
2018-05-16
Start date
2016-10-02
Completion date
Unknown
Last updated
2018-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck pain is the fourth leading cause of disability in middle age. Several factors link to the etiology of neck pain, and myofascial trigger points is the common reason for chronic neck pain. Musculoskeletal Diseases

Interventions

The clinical data of patients with chronic fascial neck pain was studied retrospectively. All the patients underwent the treatment of acupotomy, and then the muscles surrounding the cervical spine wer

Sponsors

The affiliated hospital to Changchun university of Chinese medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Subjects with neck pain 2. Suffering from neck pain for at least 3 months 3. The pain intensity was higher than 2 on a visual analogue scale (VAS) 4. Neck pain could be provoked by either neck postures or neck movement 5. Restricted cervical range of movements (flexion, extension, rotation, and side-bending) 6. Males or females aged 18 to 75 years

Exclusion criteria

Exclusion criteria: 1. Orofacial pain and temporomandibular disorders 2. A history of traumatic injuries (e.g., contusion, fracture, and whiplash injury) 3. Systemic diseases such as fibromyalgia, systemic erythematous lupus, and psoriatic arthritis 4. Neurologic disorders 5. Concomitant medical diagnosis of any primary headache (tension type or migraine) 6. Patients who had coagulopathy, abnormal findings on their ECG 7. Cervical spine surgery 8. Clinical diagnosis of cervical radiculopathy or myelopathy 9. Needle phobia

Design outcomes

Primary

MeasureTime frame
1. Degree of cervical pain, assessed using the visual analogue scale before the first treatment, immediately after the treatment and in the follow-up (1 week, 4 and 8 weeks after the last intervention) 2. Cervical range of motion, assessed before the first treatment, immediately after the treatment and in the follow-up (1 week, 4 and 8 weeks after the last intervention)

Secondary

MeasureTime frame
Psychological and disability variables, assessed using the Neck Disability Index (NDI) before the first treatment, immediately after the treatment and in the follow-up (1 week, 4 and 8 weeks after the last intervention)

Countries

China

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026