MC5-A Scrambler Therapy in Reducing Peripheral Neuropathy Caused by Chemotherapy

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
Information provided by:
Mayo Clinic
ClinicalTrials.gov Identifier:
NCT01290224
First received: February 1, 2011
Last updated: October 22, 2012
Last verified: October 2012
  Purpose

RATIONALE: Scrambler therapy may help relieve pain from peripheral neuropathy caused by chemotherapy.

PURPOSE: This phase II trial is studying how well MC5-A scrambler therapy works in reducing peripheral neuropathy caused by chemotherapy


Condition Intervention Phase
Pain
Peripheral Neuropathy
Other: scrambler therapy
Procedure: sham intervention
Other: questionnaire administration
Phase 2

Study Type: Interventional
Study Design: Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Single Blind (Subject)
Primary Purpose: Supportive Care
Official Title: Scrambler Therapy for the Treatment of Chemotherapy Induced Peripheral Neuropathy: An Evaluation of a Sham Procedure and Phase II Trial

Resource links provided by NLM:


Further study details as provided by Mayo Clinic:

Primary Outcome Measures:
  • Percentage of patients who have at least a 50% reduction (i.e., success) in at least 1 of the first 12 CIPN measurement questions in the pre/post therapy questionnaire [ Time Frame: On days 1 and 2 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Intra-patient change of CIPN symptoms between sham procedure and scrambler therapy as measured by each individual question [ Time Frame: On days 1 and 2 ] [ Designated as safety issue: No ]
  • Daily changes and percent reduction in each of the 12 CIPN measurement questions in the daily therapy questionnaire [ Time Frame: During the 10 days of recommended scrambler therapy ] [ Designated as safety issue: No ]
  • Weekly changes and percent reduction in CIPN symptoms as measured by the North Central Cancer Treatment Group (NCCTG) peripheral neuropathy question [ Time Frame: 10 weeks ] [ Designated as safety issue: No ]
  • Changes in CIPN symptom bother as measured by 8 CIPN symptom questions [ Time Frame: For 10 weeks after the scrambler therapy ] [ Designated as safety issue: No ]
  • Toxicity (other than CIPN) profile associated with scrambler therapy as measured by Common Terminology Criteria for Adverse Events (CTCAE) 4.0 [ Time Frame: By day 10 ] [ Designated as safety issue: Yes ]
  • Analgesic use in morphine equivalent units over time [ Time Frame: On days 1-11 and for 10 weeks after therapy ] [ Designated as safety issue: No ]

Estimated Enrollment: 10
Study Start Date: February 2011
Estimated Primary Completion Date: January 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Supportive Care
See Detailed Description
Other: scrambler therapy
Undergo MC5-A therapy
Other Names:
  • TENPS
  • transcutaneous electromanipulation by nervous patterns scrambler therapy
Procedure: sham intervention
Undergo sham procedure
Other: questionnaire administration
Ancillary studies

Detailed Description:

PRIMARY OBJECTIVES:

I. To explore the feasibility of studying scrambler therapy versus a sham procedure for the alleviation of lower extremity chemotherapy induced peripheral neuropathy (CIPN).

SECONDARY OBJECTIVES:

I. To obtain prospective pilot experience with recommended scrambler therapy, with regards to treatment efficacy to determine effect size estimates, patient related outcome measurement tools that we use in this trial, tolerability, and analgesic use.

OUTLINE: Patients undergo a sham procedure on the back or scrambler therapy on both lower extremities for up to 30 minutes with the Calmare MC5-A device and cutaneous electrode patches applied above and below the area of pain on days 1 and 2. Patients continue scrambler therapy for 10 days in the absence of unacceptable toxicity.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Received neurotoxic chemotherapy (including taxanes-such as paclitaxel or docetaxel, or platinum-based compounds such as carboplatin or cis-platinum or oxaliplatin, or vinca alkaloids such as vincristine, vinblastine, or vinorelbine, or proteosome inhibitors such as bortezomib); Note: this neurotoxic chemotherapy must have been completed more than 3 months prior to when they enter this trial
  • Pain or symptoms of peripheral neuropathy in the feet of >= 1 month (30 days) duration attributed to chemotherapy-induced peripheral neuropathy, for which the patient wants intervention
  • Participants have to relate that numbness, tingling or pain in their toes/feet was at least a four out of ten problem during the prior week, on a 0-10 scale where zero was no problem and ten was the worst possible problem
  • Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) = 0, 1, or 2
  • Life expectancy >= 3 months (90 days)
  • Ability to complete questionnaire(s) by themselves or with assistance
  • Provide informed written consent
  • No change in scheduled analgesic agents for at least one week

Exclusion Criteria:

  • Pregnant women
  • CIPN troubles in the lower extremities more proximal to the mid calf
  • Patients with implantable drug delivery systems, e.g. Medtronic Synchromed
  • Patients with heart stents or metal implants such as pacemakers, automatic defibrillators, aneurysm clips, vena cava clips and skull plates; (metal implants for orthopedic repair, e.g. pins, clips, plates, cages, joint replacements are allowed as are central venous access devices)
  • Patients with a history of myocardial infarction or ischemic heart disease within the past six months
  • Patients with history of epilepsy, brain damage, use of anti-convulsants, symptomatic brain metastases
  • Other identified causes of painful lower extremity paresthesias existing prior to chemotherapy (e.g., radiation or malignant plexopathy, lumbar or cervical radiculopathy, pre-existing peripheral neuropathy of another etiology: B12 deficiency, Acquired Immunodeficiency Syndrome [AIDS], monoclonal gammopathy, diabetes, heavy metal poisoning amyloidosis, syphilis, hyperthyroidism or hypothyroidism, inherited neuropathy, etc.)
  • Skin conditions such as open sores that would prevent proper application of the electrodes
  • Other medical or other condition(s) that in the opinion of the investigators might compromise the objectives of the study
  • Prior treatment with Calmare MC-5A therapy for any reason or knowledge of application procedure
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01290224

Locations
United States, Minnesota
Mayo Clinic
Rochester, Minnesota, United States, 55905
Sponsors and Collaborators
Mayo Clinic
Investigators
Study Chair: Charles Loprinzi, M.D. Mayo Clinic
  More Information

No publications provided

Responsible Party: Charles Lawrence Loprinzi, M.D., Mayo Clinic Cancer Center
ClinicalTrials.gov Identifier: NCT01290224     History of Changes
Other Study ID Numbers: MC10C8, NCI-2011-00109, 10-007874, MC10C8
Study First Received: February 1, 2011
Last Updated: October 22, 2012
Health Authority: United States: Federal Government

Additional relevant MeSH terms:
Peripheral Nervous System Diseases
Demyelinating Diseases
Polyneuropathies
Nerve Compression Syndromes
Neurologic Manifestations
Neurotoxicity Syndromes
Neuromuscular Diseases
Nervous System Diseases
Signs and Symptoms
Poisoning
Substance-Related Disorders

ClinicalTrials.gov processed this record on May 23, 2013