The Therapeutic Effect of Low-intensity Focused Ultrasound on Painful Diabetic Peripheral Neuropathy

NCT ID: NCT05624762

Last Updated: 2022-11-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-07-07

Study Completion Date

2024-01-31

Brief Summary

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Diabetic painful peripheral neuropathy (DPN) constitutes a serious threat to the outcomes of patients with diabetes. Yet, the treatments for targeting the underlying nerve damage and relieving pain are limited. The low-intensity focused ultrasound (LIFU) has been demonstrated to regulate neuronal activity without any concomitant tissue damage. Studies in animal models have shown that LIFU could protect nerve cells against inflammation and oxidative stress, as well as stimulate neurotrophic factor production. In humans, LIFU has been reported to be effective in relieving peripheral neurogenic pain caused by carpal tunnel syndrome and chemotherapy drugs. Thus, we aim to design a randomized controlled double-blind study by using LIFU. The primary endpoint is the patient's pain score (NRS), and the secondary endpoints include Neuropathy Symptom Score (NSS) and Neuropathy Deficit Score (NDS). Through this study, we anticipate establishing a new method for managing painful DPN.

Detailed Description

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Diabetic peripheral neuropathy (DPN) is a major cause of disability and mortality due to pain, loss of protective sensation, foot ulceration, amputation, and risk of falls, therefore constituting a serious threat to the outcomes of patients with diabetes and their treatment costs. The pathogenesis of DPN has been proposed as an inflammatory and oxidative stress injury in nerve cells caused by glucose and lipid metabolism disorder. Yet, the treatments for targeting the underlying nerve damage and relieving pain are limited. The widely used drugs such as Mecobalamine and Lipoic acid are not effective in some patients (about 2/3). Others, like anticonvulsant (e.g. Dabapentin), antidepressant (e.g. Duloxetine), and central opioid analgesics (e.g. Tramadol), are effective in the short-term, but they may lead to side effects for long-term use such as impairment of cognitive function, insomnia, and addiction, etc. The low-intensity focused ultrasound (LIFU) is regarded as the magnitude of ultrasonic intensity similar to or below that typically used in diagnostic ultrasound examinations. Although currently LIFU has not been applied in DPN, a number of studies have demonstrated that it can regulate neuronal activity without any concomitant tissue damage. Studies in animal models have shown that LIFU could protect nerve cells against inflammation and oxidative stress, as well as stimulate neurotrophic factor production. In humans, LIFU has been reported to be effective in relieving pain caused by carpal tunnel syndrome (Median nerve compression). Also, several studies have evidenced that cancer patients suffering from chemotherapy drug-induced peripheral neurogenic pain had significant improvement by LIFU treatment. Thus, we aim to take advantage of LIFU to treat the painful DPN. We plan to design a randomized controlled double-blind study. The primary endpoint is the patient's pain score (NRS), and the secondary endpoints include Neuropathy Symptom Score (NSS) and Neuropathy Deficit Score (NDS). Through this study, we anticipate establishing a new method for managing painful DPN.

Conditions

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Painful Diabetic Neuropathy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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LIFU group

receive LIFU therapy

Group Type ACTIVE_COMPARATOR

Low-Intensity Focused Ultrasound (LIFU)

Intervention Type DEVICE

LIFU device (LCA200; Chongqing Haifu Medical Technology Co., Ltd., Chongqing, China).

Control group

receive sham LIFU therapy

Group Type SHAM_COMPARATOR

Sham Low-Intensity Focused Ultrasound

Intervention Type DEVICE

Sham Low-Intensity Focused Ultrasound

Interventions

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Low-Intensity Focused Ultrasound (LIFU)

LIFU device (LCA200; Chongqing Haifu Medical Technology Co., Ltd., Chongqing, China).

Intervention Type DEVICE

Sham Low-Intensity Focused Ultrasound

Sham Low-Intensity Focused Ultrasound

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* age between 20 and 80 years
* having diabetes based on the criteria of the World Health Organization (WHO 1999)
* Having diabetic painful neuropathy for more than 1 month but less than 5 years
* no alcohol addiction (consumption\<140g/week in men and \<70g/week in women)
* no history of cerebral infarction/hemorrhage or other known nervous system disease
* no active infections in the skin

Exclusion Criteria

* having abnormalities in levels of Vitamin B12, Hemoglobin, and TSH.
* HbA1C\>10%
* having moderate or severe hepatic and renal dysfunctions.
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Chongqing Medical University

OTHER

Sponsor Role lead

Responsible Party

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Qian Ge

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Qian Ge, Professor

Role: STUDY_DIRECTOR

Department of Endocrinology, the First Affiliated Hospital of Chongqing Medical University

Locations

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the First Affiliated Hospital of Chongqing Medical University

Chongqing, , China

Site Status RECRUITING

Countries

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China

Central Contacts

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Qian Ge, Professor

Role: CONTACT

+8619946802662

Facility Contacts

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Qian Ge, Professor

Role: primary

+8619946802662

Other Identifiers

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DPN-China2022

Identifier Type: -

Identifier Source: org_study_id

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