Frequency Rhythmic Electrical Modulated Stimulation Effect in Peripheral Neuropathy Patients Severity of Cases and Qol.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40+
SponsorBeni-Suef University

About this trial

It's estimated that 50% of diabetic patients will have peripheral neuropathy as a complication within 3 years of the diabetes incidence \[14\], the goal of the study is to investigate this problem through the following objectives:

1. To measure the effect of using FREMS therapy in diabetic neuropathy in interventional group on the blood perfusion, neuropathy severity and quality of life after 10 sessions compared to baseline. 2. To measure the effect of using standard of care in diabetic neuropathy in control group on the blood perfusion, neuropathy severity and quality of life after 10 sessions compared to baseline. 3. To compare the results between both interventional and control group.

Eligibility criteria

Qualifiers

patients diagnosed with DM

patients age group above 40 years old.

patient diagnosed with peripheral neuropathy with symptoms lasts more than 3 months.

patients lower limb ischemia in duplex affected APSV.

Disqualifiers

patients with implant peacemakers, defibrillator, or neurostimulator.

pregnancy.

any severe disease prevent compliance to study procedures.

patients with disabilities prevent their commitment to sessions.

Trial design

Treatments tested in this trial

  • frequency rhythmic electrical modulated stimulation.
  • Duloxetine - low dose

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators