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TCMS for the Treatment of Foot Pain Caused By Diabetic Neuropathy

Primary Purpose

Diabetic Neuropathies

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
TransCutaneous Magnetic Stimulator (TCMS)
Sponsored by
University of Maryland, Baltimore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Neuropathies

Eligibility Criteria

18 Years - 89 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age ≥ 18 years of age.
  2. Prescription pharmacologic treatment is insufficient for treatment of pain.
  3. Pain duration of more than one months.
  4. Pain occurs daily.
  5. Chronic DN associated pain that is located in bilateral feet and is not explained by a central anatomic nerve compression and can clearly be correlated with that patient's history of diabetes.
  6. Pain intensity ≥ 5 in each foot at the time of enrollment.

Exclusion Criteria:

  1. Life expectancy ≤ 6 months.
  2. Oral pain medication doses or active ingredient has changed significantly in the prior 2 weeks.
  3. Inability to walk at least 10 steps (with or without a cane) before and after having to sit in a chair.
  4. Another pain condition that might confound results (e.g., neuropathy from cancer chemotherapy).
  5. Inability to undergo study assessments or complete questionnaires independently.
  6. Active psychological co-morbidities (i.e., uncontrolled schizophrenia)
  7. Currently using an opioid medication for the treatment of foot pain.

Sites / Locations

  • University of Maryland Center for Diabetes and Endocrinology

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment group

Arm Description

Outcomes

Primary Outcome Measures

Pain level
Numeric Pain Rating Scale, 0-10 with 0 being no pain, and 10 being worst pain ever experienced

Secondary Outcome Measures

Functional status and Patient satisfaction with treatment
Descriptive Questionnaire to asses whether participant has improved functional status, such as ability to walk and whether participant is satisfied with treatment
Changes in pain medication
Assessment of pain medications taken by participant prior to treatment and 28 days after treatment to deteremine if any of pain medications were increased, decreased or eliminated after treatment

Full Information

First Posted
July 3, 2018
Last Updated
February 17, 2022
Sponsor
University of Maryland, Baltimore
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1. Study Identification

Unique Protocol Identification Number
NCT03596203
Brief Title
TCMS for the Treatment of Foot Pain Caused By Diabetic Neuropathy
Official Title
TransCutaneous Magnetic Stimulation (TCMS) for the Treatment of Foot Pain Caused By Diabetic Neuropathy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
November 1, 2018 (Actual)
Primary Completion Date
June 30, 2019 (Actual)
Study Completion Date
July 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Maryland, Baltimore

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
The study will evaluate whether an experimental medical device that emits a series of brief, intense magnetic pulse will relieve foot pain from Diabetic Neuropathy (DN). The United States Food and Drug Administration (FDA) has approved a similar device for treatment of migraine headaches, but this type of device has not been studied for the treatment of DN.
Detailed Description
The study will evaluate whether an experimental medical device that emits a series of brief, intense magnetic pulse will relieve foot pain from Diabetic Neuropathy (DN). The United States Food and Drug Administration (FDA) has approved a similar device for treatment of migraine headaches, but this type of device has not been studied for the treatment of DN. No significant adverse reactions or side effects have been reported from the use of magnetic stimulation for the headache treatment. Some patients who have migraine headaches have excellent pain relief with the magnetic treatment even if they did not get pain relief using medications. The investigators do not know whether this magnetic treatment will relieve the foot pain caused by diabetic neuropathy, so they will test this by applying 50 strong magnet pulses to the painful area of each foot. This procedure will be repeated onto three parts of each foot. First onto the bottom of the foot, then the top of the foot and then the back of the foot including a portion of the ankle. The effect on pain in each foot while walking for about 10 steps will be recorded before the study begins and periodically for 28 days. This testing will provide data as to any improvement in pain relief. If the participants' reported pain is reduced as a result of the magnetic treatment, then the magnetic pulses will have shown that they have reduced the pain. Additional studies will be needed to further investigate this treatment and to determine how to obtain statistically significant data as to whether this therapy reduces the foot pain caused by diabetic neuropathy. One side effect of this treatment may be some muscular jerking of the foot or the leg during the application of the magnetic pulses. This jerking will last only during the treatment and will not be painful or harmful.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Neuropathies

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
17 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment group
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
TransCutaneous Magnetic Stimulator (TCMS)
Intervention Description
TCMS coils which are connected to feet and pulse generator. The generator will then be turned on to deliver 50 pulses at a pulse period of 6 seconds and at a pulse intensity of 100% to the bottom of the foot with the TCMS coil.
Primary Outcome Measure Information:
Title
Pain level
Description
Numeric Pain Rating Scale, 0-10 with 0 being no pain, and 10 being worst pain ever experienced
Time Frame
1 to 28 days
Secondary Outcome Measure Information:
Title
Functional status and Patient satisfaction with treatment
Description
Descriptive Questionnaire to asses whether participant has improved functional status, such as ability to walk and whether participant is satisfied with treatment
Time Frame
1 to 28 days
Title
Changes in pain medication
Description
Assessment of pain medications taken by participant prior to treatment and 28 days after treatment to deteremine if any of pain medications were increased, decreased or eliminated after treatment
Time Frame
1 to 28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years of age. Prescription pharmacologic treatment is insufficient for treatment of pain. Pain duration of more than one months. Pain occurs daily. Chronic DN associated pain that is located in bilateral feet and is not explained by a central anatomic nerve compression and can clearly be correlated with that patient's history of diabetes. Pain intensity ≥ 5 in each foot at the time of enrollment. Exclusion Criteria: Life expectancy ≤ 6 months. Oral pain medication doses or active ingredient has changed significantly in the prior 2 weeks. Inability to walk at least 10 steps (with or without a cane) before and after having to sit in a chair. Another pain condition that might confound results (e.g., neuropathy from cancer chemotherapy). Inability to undergo study assessments or complete questionnaires independently. Active psychological co-morbidities (i.e., uncontrolled schizophrenia) Currently using an opioid medication for the treatment of foot pain.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kashif Munir, M.D.
Organizational Affiliation
University of Maryland, Baltimore
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Maryland Center for Diabetes and Endocrinology
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34218718
Citation
Rao VP, Satyarengga M, Lamos EM, Munir KM. The Use of Transcutaneous Magnetic Stimulation to Treat Painful Diabetic Neuropathy. J Diabetes Sci Technol. 2021 Nov;15(6):1406-1407. doi: 10.1177/19322968211026943. Epub 2021 Jul 3. No abstract available.
Results Reference
derived

Learn more about this trial

TCMS for the Treatment of Foot Pain Caused By Diabetic Neuropathy

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