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Clinical Effect of LG Medipain for Managing Chronic Pain Disorders

Primary Purpose

Neuropathic Pain, Pain, Refractory Pain

Status
Recruiting
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Scrambler Therapy
Sponsored by
Jeeyoun Moon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neuropathic Pain

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Chronic pain disease (pain over 3 months) as an adult 19 years of age or older
  • Patients with 11-pointed NRS pain score ≥ 4 for the corresponding pain on the day of admission
  • Patients taking oral pain treatment drugs in the same type and dose up to 1 month before participating in the study, and taking the same medication until 1 month after participating in the study (at the time of obtaining the primary endpoint)
  • Those who voluntarily and in writing consent to participate in the study
  • A person who has agreed in writing to return the Scrambler Therapy device
  • By the classification of pain disorder, patients include with nociceptive pain such as joint pain, myofascial pain syndrome and with neuropathic pain such as postherpetic neuralgia, peripheral nerve injury and nerve entrapment syndrome and with mixed pain.

Exclusion Criteria:

  • Refusal of the patient
  • In case pain relief effect was not obtained in the past Scrambler Therapy
  • Patients currently undergoing Scrambler therapy for pain control at outpatient clinics at the Pain Center
  • Patients who had previously taken Scrambler Therapy 6 months before participating in the study
  • In case of systemic infection or local infection in the area around the treatment (the patch attachment site)
  • Patients who has cognitive decline that cannot understand the contents of the Numeric Pain Rating (NRS), questionnaire, and scrambler self application method
  • If it is difficult to self-administer 10 scrambler treatments for 2 weeks during the treatment period
  • Women during pregnancy
  • In case of implantation of a pacemaker, brain stimulator, etc.
  • Those who are not suitable for this clinical trial under the judgment of other investigators

Sites / Locations

  • Seoul National University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Nociceptive pain

Neuropathic pain

Mixed pain

Arm Description

patients with joint pain (knee and shoulder), myofascial pain syndrome

patients with postherpetic neuralgia, peripheral nerve injury (CRPS type II, brachial plexopathy, nerve entrapment syndrome)

patients with spine or SIJ origin back and buttock pain or neck pain and SPINE-origin back pain과 neck pain, SIJ-origin back and buttock pain

Outcomes

Primary Outcome Measures

Pain relief scoreobtained after 2 weeks of applying
Pain relief by NRS(Numeric rating scale): from 0(no pain) to 10(worst pain possible)

Secondary Outcome Measures

The painDETECT questionnaire (PD-Q)
The painDETECT questionnaire (PD-Q) for neuropathic pain score assessment
EuroQol-5 dimention(EQ-5D)
EuroQol-5 dimention(EQ-5D) for describing and valuing the health of life
patient global impression of change (PGIC)
patient global impression of change (PGIC) in self-report 5 scale reflects a patient's belief about the efficacy of treatment
Insomnia Severity Index
Insomnia Severity Index for assessing sleep difficulty
Oswestry Disability Index(ODI)
Oswestry Disability Index(ODI) for back & neck functional disability
The Western Ontario and McMaster Universities(WOMAC) Index
The Western Ontario and McMaster Universities(WOMAC) Index to evaluate the patient's Hip and Knee Osteoarthritis.

Full Information

First Posted
November 1, 2021
Last Updated
August 3, 2023
Sponsor
Jeeyoun Moon
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1. Study Identification

Unique Protocol Identification Number
NCT05165901
Brief Title
Clinical Effect of LG Medipain for Managing Chronic Pain Disorders
Official Title
Clinical Effect of LG Medipain for Managing Chronic Pain Disorders: A Prospective Observational Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 3, 2022 (Actual)
Primary Completion Date
January 15, 2024 (Anticipated)
Study Completion Date
January 15, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jeeyoun Moon

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Scrambler Therapy is a type of non-invasive neuromodulation. According to the researches that studied the effects of the existing Scrambler therapy, 10 times of Scrambler Therapy showed a significant pain relief lasting for more than 1-3 months in various pain disorders such as post-herpetic neuralgia, cancer-related neuropathic pain, and mixed pain. No treatment-related side effects have been reported in Scrambler therapy conducted in previous studies. The most inconvenient thing about Scrambler Therapy is that it has to be treated more than 10 times during specific period, so frequent visits to the hospital for treatment linked to the higher burden for the patient's cost and even those are not fully covered by the government's insurance. To reduce this discomfort and expand the range of treatment in the era of Corona of untact treatment, LG Electronics devised a home self-scrambler treatment device for pain patients. The LG Medipain device has the same treatment function as the existing hospital Scrambler treatment device, but there has been no study on its efficacy and safety. Therefore, the investigators want to conduct this research and find out about the safety and equal efficiency of the LG Medipain Therapy. In this study, it is expected that pain relief and improvement of quality of life can be obtained for patients with various types of chronic pain through self-application of LG Medipain device.
Detailed Description
Scrambler Therapy is a type of non-invasive neuromodulation. Scrambler Therapy is a different type of pain treatment from the theory that converts pain signals into general sensory information (non-pain signals) generated in the human body through artificial neurons and transmits them to the CNS through A-delta and C-nerve fibers, which are pain-transmitting nerve fibers. The non-pain signal converted through Scrambler Therapy exhibits a pain modulatory effect through CNS education, and eventually, the pain signal is continuously disturbed into a pain-free signal, resulting in pain relief. This will function to normalize neuronal plasticity, the cause of chronic pain, which is different from existing pain treatments based on the gate control theory that temporarily blocks or alleviates the recognition of pain stimuli in the CNS. Scrambler therapy is similar to the existing TENS treatment, but the treatment process is very different from TENS. TENS is a principle that replaces the delivery of pain stimulus to the brain with a stimulus other than pain stimulus and transmits it to the brain. However, Scrambler Therapy is a treatment that reduces the perception of pain in the brain by scrambling the conversion of pain stimulation into electrical signals in the peripheral nerves, similar to TENS, but can convert pain signals into pain-free signals through repetitive brain learning. So to speak, the investigators could state that it is a treatment method that fundamentally suppresses the generation of pain signals. According to the researches that studied the effects of the existing Scrambler therapy, 10 times of Scrambler Therapy showed a significant pain relief lasting for more than 1-3 months in various pain disorders such as post-herpetic neuralgia, cancer-related neuropathic pain, and mixed pain. No treatment-related side effects have been reported in Scrambler therapy conducted in previous studies. The most inconvenient thing about Scrambler Therapy is that it has to be treated more than 10 times during specific period, so frequent visits to the hospital for treatment linked to the higher burden for the patient's cost and even those are not fully covered by the government's insurance. To reduce this discomfort and expand the range of treatment in the era of Corona of untact treatment, LG Electronics devised a home self-scrambler treatment device, LG Medipain for pain patients. While the hospital Scrambler Therapy device uses up to 5 channels (with 10 patches attached) for treatment and the size of the machine is large, the LG Medipain device uses 2 channels (up to 4 patches attached) and is portable and easy to use which is designed to be convenient. The LG Medipain device has the same treatment function as the existing hospital Scrambler treatment device, but there has been no study on its efficacy and safety. Therefore, the investigators want to conduct this research and find out about the safety and equal efficiency of the LG Medipain Therapy. In addition, in order to explore the mechanism of LG Medipain treatment, 30 patients who responded to treatment will be selected and the investigators have plan to examine their EEG waveform of 32 channel with their consents. After 2 weeks of applying the LG Medipain Therapy for various chronic pain diseases, meaningful (MCD 30% for each group) pain relief effect will be obtained. The purpose of this study is to check whether pain relief can be obtained after 2 weeks of applying 10 times of the LG Medipain therapy for various chronic pain diseases. The secondary purpose of this study is to compare the pain and related-function improvement effects of the LG Medipain Therapy by pain classification. Scrambler treatment has been reported to have a pain relief effect on postherpetic neuralgia, various cancer pains, and musculoskeletal pain through basic 10 applications. In this study, it is expected that pain relief and improvement of quality of life can be obtained for patients with various types of chronic pain through self-application of the LG Medipain device.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neuropathic Pain, Pain, Refractory Pain, Chronic Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
3 different chronic pain classification
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Nociceptive pain
Arm Type
Experimental
Arm Description
patients with joint pain (knee and shoulder), myofascial pain syndrome
Arm Title
Neuropathic pain
Arm Type
Experimental
Arm Description
patients with postherpetic neuralgia, peripheral nerve injury (CRPS type II, brachial plexopathy, nerve entrapment syndrome)
Arm Title
Mixed pain
Arm Type
Experimental
Arm Description
patients with spine or SIJ origin back and buttock pain or neck pain and SPINE-origin back pain과 neck pain, SIJ-origin back and buttock pain
Intervention Type
Device
Intervention Name(s)
Scrambler Therapy
Intervention Description
LG Medipain is a type of non-invasive neuromodulation.
Primary Outcome Measure Information:
Title
Pain relief scoreobtained after 2 weeks of applying
Description
Pain relief by NRS(Numeric rating scale): from 0(no pain) to 10(worst pain possible)
Time Frame
after 2 weeks of applying
Secondary Outcome Measure Information:
Title
The painDETECT questionnaire (PD-Q)
Description
The painDETECT questionnaire (PD-Q) for neuropathic pain score assessment
Time Frame
during 1 year of treatment
Title
EuroQol-5 dimention(EQ-5D)
Description
EuroQol-5 dimention(EQ-5D) for describing and valuing the health of life
Time Frame
during 1 year of treatment
Title
patient global impression of change (PGIC)
Description
patient global impression of change (PGIC) in self-report 5 scale reflects a patient's belief about the efficacy of treatment
Time Frame
during 1 year of treatment
Title
Insomnia Severity Index
Description
Insomnia Severity Index for assessing sleep difficulty
Time Frame
during 1 year of treatment
Title
Oswestry Disability Index(ODI)
Description
Oswestry Disability Index(ODI) for back & neck functional disability
Time Frame
during 1 year of treatment
Title
The Western Ontario and McMaster Universities(WOMAC) Index
Description
The Western Ontario and McMaster Universities(WOMAC) Index to evaluate the patient's Hip and Knee Osteoarthritis.
Time Frame
during 1 year of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Chronic pain disease (pain over 3 months) as an adult 19 years of age or older Patients with 11-pointed NRS pain score ≥ 4 for the corresponding pain on the day of admission Patients taking oral pain treatment drugs in the same type and dose up to 1 month before participating in the study, and taking the same medication until 1 month after participating in the study (at the time of obtaining the primary endpoint) Those who voluntarily and in writing consent to participate in the study A person who has agreed in writing to return the Scrambler Therapy device By the classification of pain disorder, patients include with nociceptive pain such as joint pain, myofascial pain syndrome and with neuropathic pain such as postherpetic neuralgia, peripheral nerve injury and nerve entrapment syndrome and with mixed pain. Exclusion Criteria: Refusal of the patient In case pain relief effect was not obtained in the past Scrambler Therapy Patients currently undergoing Scrambler therapy for pain control at outpatient clinics at the Pain Center Patients who had previously taken Scrambler Therapy 6 months before participating in the study In case of systemic infection or local infection in the area around the treatment (the patch attachment site) Patients who has cognitive decline that cannot understand the contents of the Numeric Pain Rating (NRS), questionnaire, and scrambler self application method If it is difficult to self-administer 10 scrambler treatments for 2 weeks during the treatment period Women during pregnancy In case of implantation of a pacemaker, brain stimulator, etc. Those who are not suitable for this clinical trial under the judgment of other investigators
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jee Yoon Moon, Pf
Phone
+82 2 2072 2462
Email
jymoon0901@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jee Yoon Moon, Pf
Organizational Affiliation
Seoul national universitiy Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Seoul National University Hospital
City
Seoul
ZIP/Postal Code
110-744
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jee Y Moon, PhD
Phone
+82 2 2072 2462
Email
jymoon0901@gmail.com
First Name & Middle Initial & Last Name & Degree
Jee Y Moon, PhD

12. IPD Sharing Statement

Plan to Share IPD
No

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Clinical Effect of LG Medipain for Managing Chronic Pain Disorders

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