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Electrolysis in Patients With Low Back Pain

NCT06661070 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2024-10-28

No results posted yet for this study

Summary

The goal of this observational study is to investigate the efficacy of percutaneous electrolysis compared with dry needling on pain sensations and multifidus muscle properties in subjects with low back pain. The main questions it aims to answer are:

The high-intensity and low-intensity percutaneous electrolysis may induce pressure pain threshold (PPT) changes in myofascial trigger points in the low back during the intervention compared with dry needling.

Percutaneous electrolysis interventions may reduce stiffness in the multifidus muscle during the intervention compared with dry needling.

Conditions

  • Low Back Pain

Interventions

DEVICE

Electrolysis Percutaneous Therapeutic (EPTE)

EPTE device (Ionclinics, Valencia, Spain)

OTHER

Dry Needling

A dry needle with size 0.30 × 40 (Agupunt, Barcelona, Spain)

Sponsors & Collaborators

  • Universidad Complutense de Madrid

    collaborator OTHER

  • Universidad Rey Juan Carlos

    collaborator OTHER

  • Wroclaw University of Health and Sport Sciences

    lead OTHER

Principal Investigators

  • Juan Antonio Valera-Calero, PhD · Universidad Complutense de Madrid

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
35 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-04
Primary Completion
2024-11-23
Completion
2024-11-23

Countries

  • Spain

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 NCT06661070 on ClinicalTrials.gov