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Efficacy of Noninvasive Radiofrequency in Attenuating Diabetic Neuropathic Pain

Efficacy of Capacitive-Resistive Noninvasive Radiofrequency in Improving Perfusion Index and Attenuating Diabetic Neuropathic Pain; A Pre-post Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05917249
Enrollment
23
Registered
2023-06-23
Start date
2023-06-07
Completion date
2024-01-30
Last updated
2024-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic Neuropathy, Painful

Brief summary

Peripheral neuropathy increases the prevalence of diabetic foot ulcers following a decrease in foot sensation. Therefore, the treatment of this disorder is very important.

Detailed description

The current study aimed to investigate the efficacy of TECAR therapy on lower limb perfusion index (PI) and to evaluate the efficacy of TECAR therapy in improving the peripheral vascularity, reducing foot pain, and improving the tactile sensation of the soles in diabetic peripheral neuropathy (DPN) patients. twenty three diabetic neuropathy patients were included in the study and underwent 12 sessions of Capacitive TECAR therapy over one month. Pain, tactile sensation of the sole and PI were evaluated at the start and after each session till the end of the study.

Interventions

DEVICECapacitive-Resistive Noninvasive Radiofrequency

The two passive plates were under the back of the patient. The active capacitive plates of the machine (CAPENGERY, C200, Spain) will be applied initially for 20 minutes over the sole of both feet, with the machine adjusted on the A-thermal mode (37 oC). During the remaining 20 minutes, active capacitive plates are relocated over femoral vessels at the femoral triangle with the machine adjusted on the frank thermal mode (41 oC).

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Age 40-70 years * Type II DM with DPN (grade I-II) in lower limbs * Duration of DM\>5 years * Visual Analog Scale (VAS) ≥3 in the feet * Sensory impairments in the lower extremities

Exclusion criteria

* Patient with previous stenting or surgical intervention of lower limb arterial system. * Patients with previous history of DVT. * Pregnancy * Diabetic infectious wound * Cardiac pacemaker presence * Severe liver and kidney dysfunction or history of heart and lung disease.

Design outcomes

Primary

MeasureTime frameDescription
Change of the perfusion index at the end of the first session compared to baseline readings.40 minutesthe perfusion index readings will be taken before the first session and set as baseline reading and after the first session and the change will be calculated.The Masimo SET Mighty-Sat Fingertip Pulse Oximetry (Masimo Corporation, Irvine, CA, USA model 9900) was attached to the big toe of each patient. the reading will be the the mean of three measurements of perfusion index (PI) taken at one-minute intervals.

Secondary

MeasureTime frameDescription
Visual Analogue Scale2 monthsPatient defines the degree of pain on a visual scale without numeric values, while the values are visible on the back side for the registrar where 0 indicates no pain and 10 indicates the most unbearable pain. The test was performed before intervention, after each session and one month after the end of all twelve sessions.
Tactile sensation of the sole2 monthsTactile sensation of the sole using Semmes-Weinstein monofilament 5.07/10 g. the test will be performed after each session.
Analgesic effect2 months* Analgesic effect after each session; will be evaluated using the four grades of WHO evaluation criteria for pain relief: * Complete remission (CR) * Partial remission (PR) * Mild remission (MR) * No response (NR).
The total remission rate2 months

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026