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Cannabis Vs Opioids Pain Management Objective Testing Comparisons (CVO)

Primary Purpose

Chronic Pain, Circulatory Disorders

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Monochromatic Infrared Photo Energy (MIRE)
Transcutaneous Electrical Nerve Stimulation
Opioids
Cannabis
Sponsored by
American Association of Sensory Electrodiagnostic Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Pain

Eligibility Criteria

undefined - 90 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • In the investigator's judgment a high probability of 5 year survival.
  • Patient is able to comply with the study visit schedule.
  • Patient has the ability to comprehend and sign an informed consent document prior to study enrollment.

Exclusion Criteria:

  • In the investigator's judgment not a high probability of 5 year survival.
  • Patient is unable to comply with the study visit schedule.
  • Patient does not have the ability to comprehend and sign an informed consent document prior to study enrollment.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Other

    Arm Label

    Objective Nerve Conduction testing

    Arm Description

    Therapy of chronic pain and swelling with Monochromatic Infrared Photo Energy (MIRE) in combination with Transcutaneous Electrical Nerve Stimulation (TENS) and Cannabis or Opioids, to determine which treatment is deemed as the most successful, through objective nerve conduction testing with Neural Scan or AXON-II testing systems. Other types of therapies may be introduced during comparison reviews.

    Outcomes

    Primary Outcome Measures

    Change in pain and swelling, as verified by objective nerve conduction testing
    To note changes in axon nerve firings obtained by nerve amplitude measurements. Categorize pain and swelling disorders' treatment success or failure, as defined within the AASEM, using the Neural Scan or AXON-II objective nerve conduction testing systems, with objective responses

    Secondary Outcome Measures

    Full Information

    First Posted
    October 23, 2018
    Last Updated
    October 3, 2023
    Sponsor
    American Association of Sensory Electrodiagnostic Medicine
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03734731
    Brief Title
    Cannabis Vs Opioids Pain Management Objective Testing Comparisons
    Acronym
    CVO
    Official Title
    Clinical Trial Policy Study for the Objective Comparison of Cannabis Vs Opioids (CVO) Pain Management and Therapy Types for Circulatory and Chronic Pain Issues
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    February 3, 2024 (Anticipated)
    Primary Completion Date
    January 3, 2026 (Anticipated)
    Study Completion Date
    January 3, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    American Association of Sensory Electrodiagnostic Medicine

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Our purpose for the study is to find safer, less intrusive, better preforming non-addictive products, as an alternative therapy for pain relief and to help alleviate the opioid epidemic ongoing in America today.
    Detailed Description
    The AASEM nationally Sponsored/ Physicians Clinical Trial Policy CTP (Medicare study) testing results will be concluded by the Principal Investigators (MDs and DOs) of the study at each site authorized to participate by the AASEM, within the highest of scientific mathematical standards, using Pain DX Neural Scan and/or AXON II testing systems, which include amplitude testing certified with Promethius potentiometers, for Small Pain Fiber (SpF) Nerve Conduction Testing, CMS Carrier CPT codes 95904 now 95909 through 95913 units, as needed. It is expected that, at a later date, other products used for therapy and/or rehabilitation purposes will be added to the comparison protocol for the National Trial Number (NCT# TBA) assigned by the National Library of Medicine (NLM). Other products and/or DME equipment may include: infrared light therapy CPT code 97026, TENS therapy and home units CPT therapy code # 97032, as well as montmorillonite minerals for physical applications (montmorillonite is a natural mineral and has no CPT code - is not a CMS ordinarily payable event).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Pain, Circulatory Disorders

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Model Description
    Individual physician patient studies with all products and services being used on FDA label. Study process being referred to in NCD 310.1 as Clinical Trial Policy (CTP), will be approved by the Principal Investigator
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    1000 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Objective Nerve Conduction testing
    Arm Type
    Other
    Arm Description
    Therapy of chronic pain and swelling with Monochromatic Infrared Photo Energy (MIRE) in combination with Transcutaneous Electrical Nerve Stimulation (TENS) and Cannabis or Opioids, to determine which treatment is deemed as the most successful, through objective nerve conduction testing with Neural Scan or AXON-II testing systems. Other types of therapies may be introduced during comparison reviews.
    Intervention Type
    Device
    Intervention Name(s)
    Monochromatic Infrared Photo Energy (MIRE)
    Intervention Description
    Apply Monochromatic Infrared Photo Energy (MIRE) to the affected nerve
    Intervention Type
    Device
    Intervention Name(s)
    Transcutaneous Electrical Nerve Stimulation
    Intervention Description
    Apply Transcutaneous Electrical Nerve Stimulation (TENS) to the affected nerve
    Intervention Type
    Drug
    Intervention Name(s)
    Opioids
    Intervention Description
    Prescribe Opioids to treat for pain or circulatory disorders, dosage to be determined by Principal Investigator
    Intervention Type
    Drug
    Intervention Name(s)
    Cannabis
    Other Intervention Name(s)
    Marijuana
    Intervention Description
    Prescribe Cannabis to treat for pain or circulatory disorders, dosage to be determined by Principal Investigator. Comparing Opioid results to Cannabis results with objective nerve testing
    Primary Outcome Measure Information:
    Title
    Change in pain and swelling, as verified by objective nerve conduction testing
    Description
    To note changes in axon nerve firings obtained by nerve amplitude measurements. Categorize pain and swelling disorders' treatment success or failure, as defined within the AASEM, using the Neural Scan or AXON-II objective nerve conduction testing systems, with objective responses
    Time Frame
    4 to 8 weeks per nerve

    10. Eligibility

    Sex
    All
    Maximum Age & Unit of Time
    90 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: In the investigator's judgment a high probability of 5 year survival. Patient is able to comply with the study visit schedule. Patient has the ability to comprehend and sign an informed consent document prior to study enrollment. Exclusion Criteria: In the investigator's judgment not a high probability of 5 year survival. Patient is unable to comply with the study visit schedule. Patient does not have the ability to comprehend and sign an informed consent document prior to study enrollment.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Ronald F Davis
    Phone
    501-690-4028
    Email
    rondavis2227@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Brook Davis
    Phone
    501-843-4381
    Email
    nctclinicaltrial@gmail.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Ronald F Davis
    Organizational Affiliation
    AASEM/ADAPT/DTSC
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Brook Davis
    Organizational Affiliation
    ADAPT/DTSC
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    James Hedgecock, D.C., PhD
    Organizational Affiliation
    American Association of Sensory Electrodiagnostic Medicine
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Chad Pfefer, M.D.
    Organizational Affiliation
    American Association of Sensory Electrodiagnostic Medicine
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Michael F Boyer, M.D.
    Organizational Affiliation
    American Association of Sensory Electrodiagnostic Medicine
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    Through AASEM publications
    IPD Sharing Time Frame
    Annually reviews / new CME training course provided periodically during every year
    IPD Sharing Access Criteria
    Must be an AASEM certified physician/principal investigator or trial personnel. Otherwise may be obtained on AASEM website.

    Learn more about this trial

    Cannabis Vs Opioids Pain Management Objective Testing Comparisons

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