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Carpal Tunnel Syndrome and Static Magnetic Field Therapy (CTS/SMF)

Primary Purpose

Carpal Tunnel Syndrome

Status
Unknown status
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
neodymium permanent magnet
neodymium magnet
magnet
Sponsored by
National University of Natural Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Carpal Tunnel Syndrome focused on measuring static magnetic field, permanent magnet, carpal tunnel syndrome, median nerve

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Age range (18-65 years) Both genders Hand or wrist pain with paresthesias or numbness in any or all fingers, predominating in a median nerve distribution, and especially occurring at night Symptoms present for at least 3 months No prior treatment with magnet therapy Baseline BCTQ >2.0 on SSS subscale Meet specific EDX inclusion/ exclusion criteria listed in Table 1 (below) Willing and able to provide informed consent Ability to read English fluently

Exclusion Criteria:

Use of narcotic analgesia Corticosteroid injection into the carpal tunnel within previous 3 months Prior carpal tunnel surgery on affected side History of wrist or hand fracture on the symptomatic limb Skin rash or irritation on the wrist Participant (or bed partner) wearing a pacemaker or other electronic device Current pregnancy, less than 3 months postpartum, nursing, or planning a pregnancy Plans to move from area during the time frame of the study Inability to tolerate the baseline screening nerve conduction study Unable or unwilling to comply with the protocol Collecting workers' compensation or social-security disability benefits Involved in litigation regarding pain or disability Development of a rash or skin irritation to the tape applied to the wrist during a run-in baseline test period

Concomitant medical conditions including:

Insulin-dependent diabetes mellitus History of chronic renal failure or renal dialysis or forearm fistulae History of generalized peripheral neuropathy History of other neurologic disorders which may confuse the diagnosis of carpal tunnel syndrome, including but not limited to stroke, cervical radiculopathy, myelopathy, subdural hematoma, brain tumor Inflammatory articular disease or tendonitis of the involved hand or wrist Other disorders known to predispose to carpal tunnel syndrome including acromegaly, multiple myeloma, amyloidosis Cancer

Table 1. Electrodiagnostic (EDX) Inclusion and Exclusion Criteria Inclusion Criteria

  • Median nerve onset sensory latency > 3.5 ms at 13 cm
  • Median-ulnar across palm latency difference ≥ 0.4 ms
  • Median-radial to thumb latency difference ≥ 0.7 ms
  • Median-ulnar to ring finger latency difference ≥ 0.5ms ED Exclusion Criteria
  • Absent sensory nerve action potential (SNAP)
  • Median nerve distal motor latency > 6.0 ms

Sites / Locations

  • National College of Natural Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

A

B

C

Arm Description

Surface magnetic field strength at target 450 Gauss permanent magnet

Surface field strength at target 150 Gauss permanent magnet

Outcomes

Primary Outcome Measures

Boston Carpal Tunnel Questionnaire Symptom Severity Scale

Secondary Outcome Measures

1. Electrophysiological recovery of median nerve
2. General symptom questionnaire
3. Compliance with treatment

Full Information

First Posted
August 24, 2007
Last Updated
November 23, 2009
Sponsor
National University of Natural Medicine
Collaborators
National Center for Complementary and Integrative Health (NCCIH), Oregon Health and Science University
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1. Study Identification

Unique Protocol Identification Number
NCT00521495
Brief Title
Carpal Tunnel Syndrome and Static Magnetic Field Therapy
Acronym
CTS/SMF
Official Title
Carpal Tunnel Syndrome and Static Magnetic Field Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
November 2009
Overall Recruitment Status
Unknown status
Study Start Date
September 2006 (undefined)
Primary Completion Date
June 2009 (Anticipated)
Study Completion Date
August 2009 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
National University of Natural Medicine
Collaborators
National Center for Complementary and Integrative Health (NCCIH), Oregon Health and Science University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this Phase II study is to assess the feasibility of conducting a large scale trial which will evaluate the effectiveness of static magnetic field therapy as a treatment for Carpal Tunnel Syndrome. This preliminary study will determine which of three strength magnets to use in the future. Participants will be recruited from three primary sources. 1) Patients with a possible diagnosis of Carpal Tunnel Syndrome who have been referred to the Orthopaedic and Rehabilitation Clinics of OHSU for Nerve conduction studies. If after conducting these studies a potential participant shows evidence of mild to moderate Carpal Tunnel Syndrome s/he will be informed about the study and invited to participate in additional screening. B) Patients seen at the National College of Natural Medicine (NCNM) Clinics who have a clinical diagnosis of Carpal Tunnel Syndrome will be informed about the study and invited to enter the screening process for further eligibility. C) Participants will also be recruited from the general public including staff and students at OHSU and NCNM). Eligibility will be determined through a stepwise process including telephone screening for general eligibility, Nerve Conduction screening for electrodiagnostic eligibility, and Boston Carpal Tunnel Questionnaire screening for symptom severity eligibility. Those potential participants who meet all eligibility requirements will be randomized to one of three magnetic field dosages. They will be provided with a ¾" diameter x 1/8" thick magnet which they will be required to apply for six weeks during the hours of sleep. Over the course of the study participants will have four visits to the General Clinical Research Center of OHSU and three visits to the Orthopaedic and Rehabilitation Clinics of OHSU for Nerve Conduction studies to be performed by either Dr. Nels Carlson or Dr. Hans Carlson. Questionnaires to be completed during the course of the study include a general health information and demographics questionnaire, the Boston Carpal Tunnel Questionnaire, which will be completed on six occasions, a general symptoms checklist and a Post Treatment Participant satisfaction questionnaire. Recruitment, retention, compliance and safety will be analyzed using descriptive statistics. Effectiveness of the three different strength magnets will be assessed by comparing participants' baseline scores on the Boston Carpal Tunnel Questionnaire with their scores after six weeks of magnet use.
Detailed Description
See Brief Summary

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carpal Tunnel Syndrome
Keywords
static magnetic field, permanent magnet, carpal tunnel syndrome, median nerve

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
Surface magnetic field strength at target 450 Gauss permanent magnet
Arm Title
B
Arm Type
Experimental
Arm Description
Surface field strength at target 150 Gauss permanent magnet
Arm Title
C
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
neodymium permanent magnet
Intervention Description
3/4" diameter by 1/8" thick permanent magnet
Intervention Type
Device
Intervention Name(s)
neodymium magnet
Intervention Description
A. 450 Gauss static magnetic field at target B. 150 Gauss static magnetic field at target C. 0 Gauss static magnetic field at target
Intervention Type
Device
Intervention Name(s)
magnet
Intervention Description
0 Gauss magnets are worn every night during hours of sleep for 6 weeks.
Primary Outcome Measure Information:
Title
Boston Carpal Tunnel Questionnaire Symptom Severity Scale
Time Frame
Baseline, Wks 2, 4, 6, 18
Secondary Outcome Measure Information:
Title
1. Electrophysiological recovery of median nerve
Time Frame
Baseline, 6 weeks, 18 weeks
Title
2. General symptom questionnaire
Time Frame
Baseline and on completion of intervention phase
Title
3. Compliance with treatment
Time Frame
Baseline to study completion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age range (18-65 years) Both genders Hand or wrist pain with paresthesias or numbness in any or all fingers, predominating in a median nerve distribution, and especially occurring at night Symptoms present for at least 3 months No prior treatment with magnet therapy Baseline BCTQ >2.0 on SSS subscale Meet specific EDX inclusion/ exclusion criteria listed in Table 1 (below) Willing and able to provide informed consent Ability to read English fluently Exclusion Criteria: Use of narcotic analgesia Corticosteroid injection into the carpal tunnel within previous 3 months Prior carpal tunnel surgery on affected side History of wrist or hand fracture on the symptomatic limb Skin rash or irritation on the wrist Participant (or bed partner) wearing a pacemaker or other electronic device Current pregnancy, less than 3 months postpartum, nursing, or planning a pregnancy Plans to move from area during the time frame of the study Inability to tolerate the baseline screening nerve conduction study Unable or unwilling to comply with the protocol Collecting workers' compensation or social-security disability benefits Involved in litigation regarding pain or disability Development of a rash or skin irritation to the tape applied to the wrist during a run-in baseline test period Concomitant medical conditions including: Insulin-dependent diabetes mellitus History of chronic renal failure or renal dialysis or forearm fistulae History of generalized peripheral neuropathy History of other neurologic disorders which may confuse the diagnosis of carpal tunnel syndrome, including but not limited to stroke, cervical radiculopathy, myelopathy, subdural hematoma, brain tumor Inflammatory articular disease or tendonitis of the involved hand or wrist Other disorders known to predispose to carpal tunnel syndrome including acromegaly, multiple myeloma, amyloidosis Cancer Table 1. Electrodiagnostic (EDX) Inclusion and Exclusion Criteria Inclusion Criteria Median nerve onset sensory latency > 3.5 ms at 13 cm Median-ulnar across palm latency difference ≥ 0.4 ms Median-radial to thumb latency difference ≥ 0.7 ms Median-ulnar to ring finger latency difference ≥ 0.5ms ED Exclusion Criteria Absent sensory nerve action potential (SNAP) Median nerve distal motor latency > 6.0 ms
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Agatha P Colbert, MD
Organizational Affiliation
National University of Natural Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
National College of Natural Medicine
City
Portland
State/Province
Oregon
ZIP/Postal Code
97201
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
20599049
Citation
Colbert AP, Markov MS, Carlson N, Gregory WL, Carlson H, Elmer PJ. Static magnetic field therapy for carpal tunnel syndrome: a feasibility study. Arch Phys Med Rehabil. 2010 Jul;91(7):1098-104. doi: 10.1016/j.apmr.2010.02.013.
Results Reference
derived

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Carpal Tunnel Syndrome and Static Magnetic Field Therapy

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