Percutaneous Needle Electrolysis on Metatarsalgia

University of Seville

Status: Enrolling

Conditions: Metatarsalgia

Treatments: Other: Conservatory treatment; Other: Innovate treatment

Study type: Interventional

Funder types: Other

Identifiers

NCT05262972

PNE and metatarsalgia

Details and patient eligibility

About

Percutaneous electrolysis is a minimally invasive method that involves the application of a galvanic current through an acupuncture needle. The needle is placed directly into the soft tissue structures, essential with ultrasound guidance. This technique involves the combination of mechanical stimulation produced by the needle and electrical/biochemical stimulation provided by the electrical current.

Endogenous pain modulation shows clinical relevance of this technique and plays an important role in the experience of pain.

Plantar plate injury is a pathology that frequently occurs in the forefoot, especially in middle-aged women, causing metatarsalgia that is sometimes very intense. In most cases it is secondary to a mechanical imbalance of the forefoot, related to an insufficiency of the first radius. For this reason, the researchers hypothesize that the application of ultrasound-guided percutaneous electrolysis on the plantar plate, combined with the conservative treatment consisting of the development of a personalized plantar orthosis, can cause positive effects in the patient's clinic as well as improve their quality of life.

Enrollment: 30 estimated patients

Sex: Female

Ages: 40 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Adult female patients (40-65 years old)
• Having pain in the 2nd MTP joint of the foot due to pathology of the plantar plate, diagnosed by a specialized professional.

Exclusion criteria

• to have suffered an injury to their musculoskeletal system in the last 6 months.
• to have the present neuritic pathology,
• to have complete rupture of the plantar plate, 2nd finger supraadductus, flexor digitorum longus tenosynovitis,
• to have problems in the lumbar spine,
• to have undergone surgery in the lumbar spine or lower limbs.
• to use a plantar orthosis.
• to have the presence of associated pathologies in the foot,
• to be under the influence of any medication at the time of the study, fear of needles
• to be pregnant
• to be epileptic.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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30 participants in 2 patient groups

Group I

Experimental group

Description:

The subject will obtain a conservative treatment for this type of pathology consisting of the development of a personalized plantar orthosis

Treatment:

Other: Conservatory treatment

Group II

Experimental group

Description:

The subjects belonging to this group, in addition to providing their corresponding personalized plantar orthosis, will receive a complementary treatment consisting of the application of ultrasound-guided percutaneous electrolysis

Treatment:

Other: Innovate treatment