Effect of Electroacupuncture on Sensitive Symptoms of Distal Diabetic Peripheral Neuropathy
- Conditions
- ElectroacupunctureAcupunctureDiabetic PolyneuropathyNerve ConductionDiabetic Peripheral Neuropathic PainDiabetic Peripheral Neuropathy
- Interventions
- Procedure: Sham AcupunctureProcedure: Electroacupuncture
- Registration Number
- NCT05521737
- Lead Sponsor
- Instituto Mexicano del Seguro Social
- Brief Summary
This is a controlled clinical trial with the aim to study the effects of electroacupuncture on neuropathic pain reduction, quality of life and changes in sensory and motor nerve conduction velocity in patients with type 2 diabetes mellitus, beneficiaries of the familiar medical centers 20, 40 and 41 of the Instituto Mexicano del Seguro Social, at north of Mexico City, in colaboration with the human acupuncture specialty of the Escuela Nacional de Medicina y Homeopatía, Instituto Politécnico Nacional, Mexico.
- Detailed Description
Controlled clinical trial to evaluate the effect of electroacupuncture on the reduction of neuropathic pain, quality of life; electrophysiological, inflammatory response, oxidative stress, and genetic expression, in patients with type 2 diabetes mellitus, beneficiaries from the family medical centers 20 , 40 and 41 of the Instituto Mexicano del Seguro Social, at north of Mexico City.
Once the acceptance letter has been signed, a series of questionnaires (MNSI, MDNS, DN-4, NRS, and SF-36), and a physical examination will be carried out to meet the necessary criteria to continue participating.
Only candidates with clinical diagnosis of diabetic polyneuropathy will have an electrophysiological examination by nerve conduction velocity study, if so, patients will be randomized to the electroacupunture or sham acupuncture groups.
Before intervention, laboratory studies will be taken after fasting for 8 to 10 hours, to determine biochemichal profile (glucose, urea, creatinine, uric acid , triglycerides, total cholesterol, HDL and LDL), oxidative stress (Malondialdehyde), inflammatory response (IL-6, IL1β, TNF-α, IL-10 and IL-18 cytokines), and gene expression (5-HT1AR, Neurokinin 1, α-adrenoreceptors, NGF, CX3CR1, GAP-43, and NT3).
Intervention will be applied in a total of 32 acupuncture sessions, divided into two intervention cycles, that is, 16 sessions over two months, with a rest period of one month in between.
At the end of both cycles of interventions, the questionnaires, the nerve conduction velocity study the biochemical and molecular studies will be re-assessed. Finally, this will be re-evaluated after three months post-intervention in order to evaluate the effect of intervention over time.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 200
- Patients with type 2 diabetes.
- Patients with clinical diabetic peripheral polyneuropathy.
- Patients with electrophysiological diagnosis of diabetic peripheral polyneuropathy in its different types of classification.
- Type 1 Diabetes or gestational diabetes.
- Systemic autoimmune diseases.
- Hematological disorders.
- HIV diagnosis.
- Cancer in treatment.
- Pregnancy.
- Other types of neurological disorders or neuropathies.
- Intervention with acupuncture six months previously.
- Patients with pacemarkers.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Sham group Sham Acupuncture Sham acupuncture will be administered in a total of 32 sessions within five months. Interventional group Electroacupuncture Electroacupuncture will be administered in a total of 32 sessions within five months.
- Primary Outcome Measures
Name Time Method Nerve Conduction Velocity Baseline evaluation, after the first and second cycle of intervention, respectively, and three months after the end of the intervention. Measured by Nerve Conduction Velocity Study using the VIKING LIFE-SAVING EQUIPMENT, to determine Motor and Sensitive Nerve Conduction Velocity of common peroneal nerve, sural nerve, and tibial nerve.
Sensitive Nerve Conduction (SCV). Distance between the receiving point and the stimulus point. SCV normal values: Peroneal nerve ≥ 41 m/s, tibial nerve ≥ 44 m/s, sural nerve ≥ 50 m/s.
Motor Conduction Velocity (MCV). Distance between two points and the difference in incubation between them after superstimulation of the corresponding nerve branch. MCV normal values: Peroneal nerve ≥ 41 m/s, tibial nerve ≥ 44 m/s, sural nerve ≥ 60 m/s.
\*Values below those stipulated above indicate that NCV has slowed down, and is abnomal.
The investigators expect a diminishment of SCV and MCV in sham acupuncture group from the first cycle of intervention whereas electroacupuncture group remains unchanged or even increases SCV and MCV.
- Secondary Outcome Measures
Name Time Method Michigan Neuropathy Screening Instrument (MNSI). Baseline evaluation, after the first and second cycle of intervention, respectively, and three months after the end of the intervention. It will be assessed with a lower extremity examination by a health professional of both feet in search of deformities, dry skin, calluses, infections, fissures and ulcers. Complemented with measurement of vibratory sensation, ankle reflexes, and Semmes-Weinstein monofilament test.
The investigators expect improvement in the physical aspect of the foot in the electroacupuncture group, while in the sham acupuncture group the complication progresses.Michigan Diabetic Neuropathy Score (MDNS) Baseline evaluation, after the first and second cycle of intervention, respectively, and three months after the end of the intervention. Composed of three items where the sensory compromise is evaluated with the perception of vibration, 10 gr. monofilament and pin prick, in addition to the muscular strength of the toes, and the bicipital, tricipital, quadriceps and achilles muscle reflexes. The investigators expect a diminishment of MDNS score and clinical improvement in the electroacupuncture group and progression of clinical manifestations in the sham group.
Douleur Neuropathique en 4 Questions (DN-4) Baseline evaluation, after the first and second cycle of intervention, respectively, and three months after the end of the intervention. A screening tool for neuropathic pain consisting of 10 interview questions (DN4-interview) and physical tests. A score greater than 4 points suggests neuropathic pain. The investigators expect decreased scores in the electroacupuncture group and increased or persistent scores in the sham group.
Numerical Pain Rating Scale (NRS) Baseline evaluation, after the first and second cycle of intervention, respectively, and three months after the end of the intervention. Patients are only asked to circle the number between 0 and 10, 0 and 20 or 0 and 100 that best matches the intensity of their pain currently and in the last 7 days, where zero usually represents "no pain", while the upper limit represents "the worst pain of their life". The investigators expect diminishment of rating scale in electroacupuncture group and an increase in sham acupuncture group.
Quality life (SF-36) Baseline evaluation, after the first and second cycle of intervention, respectively, and three months after the end of the intervention. It will be measured by The Short Form-36 Health Survey (SF-36) a measure of health status that consists of eight scaled scores (vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, and mental health), which are the weighted sums of the questions in their section. The investigators expect quality life improvement in electroacupuncture group while in sham acupuncture group might worsen.
Oxidative Stress Baseline evaluation, after the first and second cycle of intervention, respectively, and three months after the end of the intervention. Determined by quantifying the concentrations of the lipoperoxidation product Malondialdehyde (MDA). An increase of MDA is expected in the sham group, while in the electroacupuncture group it is expected to decrease.
Inflammatory response Baseline evaluation, after the first and second cycle of intervention, respectively, and three months after the end of the intervention. Assessed by changes in serum concentrations of proinflammatory (IL-6, IL1β, TNF-α and IL-18) and anti-inflammatory (IL-10) cytokines determined by quantitative ELISA by flow cytometry. The investigators expect increase of anti-inflammatory cytokine and decrease of proinflammatory cytokines in the electroacupuncture group, while in the sham group this is inversely presented.
Genetic expression Baseline evaluation, after the first and second cycle of intervention, respectively, and three months after the end of the intervention. mRNA expression of 5-HT1AR, Neurokinin 1, α-adrenoreceptors, NGF (Nerve growth factor), CX3CR1, GAP-43 (Growth associated protein 43) and Neurotrophin (NT3), (Chemoline receptor 1) genes quantified by real-time PCR. The investigators expect an increase in gene expression in patients with electroacupuncture while in sham patients it is decreased or even unchanged.
Trial Locations
- Locations (1)
Medical research unit in biochemistry, UMAE "Dr. Bernardo Sepúlveda".Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social.
🇲🇽Mexico City, Cuauhtémoc, Mexico