Cupping Therapy for Neck Pain in Cervical Spondylosis

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-60
SponsorUniversity of Medicine and Pharmacy at Ho Chi Minh City

About this trial

Cervical spondylosis is one of the common causes of chronic neck pain. It can significantly affect the quality of life, lead to disabilities, and increase the economic burden on patients. Treatment mainly includes pain relievers, non-steroidal anti-inflammatory drugs (NSAIDs), muscle relaxants or physical therapy. The condition tends to recur frequently; therefore, long-term use of medication can lead to unwanted effects on the digestive system, kidneys, and cardiovascular system.

Dry cupping therapy is a non-pharmacological method that has been shown to be effective in pain management. Cupping therapy has the advantage of being applicable to patients who are afraid of needles and has a wide area of effect.

Given the limitations in evaluating treatment effectiveness and safety, along with the lack of published research discussing the analgesic effects of dry cupping for neck pain caused by cervical spondylosis, the investigators conducted the study on pain reduction and safety of cupping therapy in patients with neck pain caused by cervical spondylosis.

Eligibility criteria

Qualifiers

Individuals between the ages of 20 and 60 years, outpatient treatment.

Individuals diagnosed with cervical spondylosis.

Individuals report pain intensity between 3 and 8 according to on the Visual Analogue Scale (VAS) on the screening visit day.

Experiencing neck pain for no longer than four weeks.

Disqualifiers

Patients diagnosed with acute or chronic neck pain due to specific causes or with root compression syndrome, spinal cord compression syndrome, or vertebral artery syndrome.

Patients loss of normal cervical curvature or deformity.

Individuals with a history of neck trauma, cervical vertebra fracture, or cervical spine surgery, congenital spinal abnormalities, systemic bone and joint diseases.

Patients have undergone cupping therapy, plastering, or drug inhalation within one week prior to participating in the study.

Trial design

Treatments tested in this trial

  • Dry cupping therapy
  • Electroacupuncture

Treatment groups

82 Participants
are divided into 2 treatment groups

Locations

This trial has no locations