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Focal Microvibration and Chronic Lumbosacral Radicular Pain

Unknown statusNot applicableNCT06301061
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The goal of this clinical trial is to investigate the effectiveness of focal microvibration on patients affected by chronic lumbosacral radicular pain. The main question\[s\] it aims to answer are: * Can focal microvibration improve pain in this patient population? * Can focal microvibration improve quality of life in these patients? Participants will attach to their skin four little devices (10x20x0,5mm) delivering focal microvibration in the painful area according to researchers indications for 6 hours/day every day except Thursday and Sunday. Researchers will compare patients treated with focal microvibration to patients treated with a sham device and to patients treated with standard pharmacological therapy.

Study details

Official title
Effectiveness of Focal Microvibration in the Management of Chronic Lumbosacral Radicular Pain: a Randomized Controlled Study
Conditions
Interventions
Sponsor
Federico II University
Start date
2024-04-01
Primary completion
2025-10-01
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Total sites listed
0

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Pain duration≥6 months * Magnetic resonance imaging (MRI) showing compression of lumbosacral nerve roots * Neuropathic symptoms in the innervation territory of the compressed spinal nerve roots * Monolateral pain * Pain intensity: moderate-severe i.e. numeric rating scale (NRS)≥4. Exclusion Criteria: * Psychiatric patients * Cancer patients * Patients affected by disease characterized by spasticity or muscular stiffness: Parkinson's disease, multiple sclerosis, stroke, spine injuries. * Patients with spinal or dorsal root ganglion stimulators * Patients undergone central of peripheral stimulation in the past 3 months * Patients affected by fibromyalgia. * Patients undergone central nervous system surgery * Patients with reduced renal function eGFR≤60ml/min/1,73m2

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06301061