Metatarsalgia
Conditions
Brief summary
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.
Interventions
Personalized plantar orthosis
OTHERInnovate treatment
Personalized plantar orthosis + percutaneous electrolysis
Sponsors
University of Seville
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
40 Years to 65 Years
Healthy volunteers
Yes
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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Quality of life | 1 month | Foot Health Status Questionnaire |
| Subjetive level of pain | 1 month | Intensity of subjective pain in the injured structure (0, no pain; 10, worse pain) |
| level of pain at palpation | 1 month | Intensity of pain on palpation in the injured structure (0, no pain; 10, worse pain) |
| Distribution of plantar pressures | 1 month | Podiatric platform (pressure percentage 0-100%) |
Countries
Spain
Contacts
Primary ContactBlanca De la Cruz Torres, Dr
Outcome results
None listed