Effect of Electroacupuncture on Sensitive Symptoms of Distal Diabetic Peripheral Neuropathy

NCT05521737 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2024-05-22

No results posted yet for this study

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.

Conditions

  • Electroacupuncture
  • Acupuncture
  • Diabetic Polyneuropathy
  • Diabetic Peripheral Neuropathy
  • Diabetic Peripheral Neuropathic Pain
  • Nerve Conduction

Interventions

PROCEDURE

Electroacupuncture

Intervention consists of a total of 32 sessions, divided into two intervention cycles, that is, 16 sessions over two months, with a rest period of one month in between. EA is applied for 20 minutes at an alternating frequency of 2 Hz. Acupunctural points are Zusanli (E36), Fenlong (E40), Yinlingquan (B9), Sanyinjiao (B6), Taichong (H3) and Zulinqi (VB41).

PROCEDURE

Sham Acupuncture

Intervention consists of a total of 32 sessions, divided into two intervention cycles, that is, 16 sessions over two months, with a rest period of one month in between. Sham acupuncture will be applied using a nonpuncture device without electrical stimulation at the same acupunctural points as in the EA group.

Sponsors & Collaborators

  • National Polytechnic Institute, Mexico

    collaborator OTHER
  • Instituto Nacional de Salud Publica, Mexico

    collaborator OTHER
  • Escuela Superior de Medicina, Instituto Politécnico Nacional

    collaborator UNKNOWN
  • Escuela Nacional de Medicina y Homeopatía, Instituto Politécnico Nacional

    collaborator UNKNOWN
  • Universidad Nacional Autonoma de Mexico

    collaborator OTHER
  • Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de Mexico

    collaborator UNKNOWN
  • Facultad de Estudios Superiores Zaragoza, Universidad Nacional Autónoma de Mexico

    collaborator UNKNOWN
  • Facultad de Medicina, UNAM

    collaborator UNKNOWN
  • Instituto Mexicano del Seguro Social

    lead OTHER_GOV

Principal Investigators

  • José de Jesús Peralta Romero, PhD · Instituto Mexicano del Seguro Social

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-11-01
Primary Completion
2024-12-31
Completion
2025-12-31

Countries

  • Mexico

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05521737 on ClinicalTrials.gov