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Efficacy of eletroacupuncture in muscular pain

Efficacy of Intramuscular Stimulation Techniques to Treat Chronic Myofascial Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-43r7rf
Enrollment
Unknown
Registered
2017-04-18
Start date
2016-08-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Myofascial Pain

Interventions

Dry needling group: 30 patients will be submitted to the dry needling of the trigger point of the upper trapezius muscle Trigger point electrostimulation group: 30 patients will be submitted to trigge
Procedure/surgery

Sponsors

Universidade Estadual Paulista "Julio de Mesquita Filho" Faculdade de Medicina de Botucatu
Lead Sponsor
Universidade Estadual Paulista "Julio de Mesquita Filho" Faculdade de Medicina de Botucatu
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: older than 18 years; history of musculoskeletal pain for three months or more; presence of active myofascial trigger points in the upper trapezius muscle in the evaluation; presence of referred pain at the trigger point equal to or greater than three on the Visual Analogue Pain Scale (VAS) for at least five days pre-treatment

Exclusion criteria

Exclusion criteria: cervicobrachialgia for radiculopathy proven by clinical evaluation, neurological signs and / or imaging tests (CT or MRI); patients with diabetes mellitus and other neuropathies; use of opioids and / or other drug therapies less than 1 month; signs and symptoms that meet diagnostic criteria for fibromyalgia; contraindications for the use of electrical stimulation (pacemaker patients, other electro-stimulators); patients taking anticoagulant medication

Design outcomes

Primary

MeasureTime frame
To prove the superiority of the motor-point stimulation technique in Myofascial Syndrome for pain relief measured through visual analogue scale (VAS) measured through visual analogue scale (EVA) and pain questionnaire at the end of 8 sessions.

Secondary

MeasureTime frame
To show improvement in the physical and mental health and quality of life of the patients after the treatment of Myofascial Syndrome through physical and mental health questionnaires with the techniques used at the end of 8 sessions.

Countries

Brazil

Contacts

Public ContactMarlene Moro

Universidade Estadual Paulista Julio de Mesquita Filho Faculdade de Medicina de Botucatu

marlenemoro@uol.com.br+55-014-32241040

Outcome results

None listed

Source: REBEC (via WHO ICTRP)