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Trial record 1 of 1 for:    NCT03195270
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Use of PET/MR Imaging in Chronic Pain

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ClinicalTrials.gov Identifier: NCT03195270
Recruitment Status : Recruiting
First Posted : June 22, 2017
Last Update Posted : November 3, 2022
GE Healthcare
Information provided by (Responsible Party):
Feliks Kogan, Stanford University

Brief Summary:
The investigators are studying the ability of PET/MR imaging (using the PET tracer [18F]FDG) to objectively identify and characterize pain generators in patients suffering from chronic pain.

Condition or disease Intervention/treatment Phase
Chronic Pain Drug: [18F]FDG Device: PET/MRI Phase 1

Detailed Description:

The diagnosis and management of chronic and neuropathic pain syndromes remains a major clinical challenge, and this failure is partly attributed to our inability to identify the hypersensitive and inflammatory changes in the pain-sensing part of our nervous system that is thought to contribute to these syndromes. The lack of a specific, objective diagnostic test for chronic and neuropathic pain syndromes can result in a delay of diagnosis and suboptimal management decisions. This delay in diagnosis is quite unfortunate since the early diagnosis and treatment of a disease is attributed to the highest probability of remission in certain chronic pain syndromes. Additionally, identifying the correct source of pain is of paramount importance since the clinical course and therapeutic interventions are different depending on cause.

Evidence in the literature points strongly toward an active inflammatory component in chronic pain. For example, soft tissue and bony inflammation is known to be an important pathophysiological mechanism for the symptoms of certain neuropathic pain syndromes. Similarly, individuals suffering from chronic sciatica or radiculopathy may suffer from a combination of inflammation and compression of lumbar or cervical spinal nerves. It is also established that inflammatory lesions have increased metabolism and energy requirements and, therefore, are more glucose-avid than normal tissues, showing increased uptake of radiolabeled glucose analogs, such as [18F]fluorodeoxyglucose ([18F]FDG). Correspondingly, [18F]FDG positron emission tomography-magnetic resonance imaging (PET/MRI) represent leading FDA-approved clinical imaging modalities to longitudinally study metabolic changes in the nervous system and non-neural tissues (e.g., muscle, blood vessels, joints, bone, scar tissue, etc.) in patients with chronic pain conditions. One of the goals of the study is to determine whether [18F]FDG PET/MRI can identify sources of inflammation with greater sensitivity, accuracy and objectivity than current diagnostic methods.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 130 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Intervention Model Description: Participants will be recruited based on established criteria for chronic pain. For the PET/MRI scan, the participants will be injected with 10 mCi±1 mCi of [18F]FTC-146 via the antecubital vein in a bolus injection. PET and MRI scans will be acquired simultaneously using a hybrid PET/MRI scanner. Following the scan, participants will be contacted to check for adverse drug events, and any events will be recorded in the case report. The biodistribution of radiotracer will be analyzed using regions of interest (ROI) marked on anatomical structures on magnetic resonance images and quantifying the signal in PET images within the same ROIs. Pharmacokinetic information will be derived using mathematical modeling. Data from chronic pain patients will be compared to historical data from asymptomatic controls.
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Use of [18F]FDG PET/MRI in the Diagnosis of Pain Generators and/or Sites of Inflammation and to Monitor Treatment Effects in Patients With Chronic Pain
Actual Study Start Date : November 24, 2014
Estimated Primary Completion Date : December 31, 2024
Estimated Study Completion Date : December 31, 2024

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: Single Arm
Drug: [18F]FDG
10 mCi of [18F]FDG via the antecubital vein in a bolus injection
Other Name: [18F]Fluorodeoxyglucose

Device: PET/MRI
PET/MRI hybrid scanner used as diagnostic device
Other Name: Positron emission tomography/magnetic resonance imaging

Primary Outcome Measures :
  1. [18F]FDG PET/MRI as a spatial biomarker for chronic pain [ Time Frame: 5 years ]
    Identification of structures with increased [18F]FDG uptake (SUVmax) corresponding to pain.

Secondary Outcome Measures :
  1. [18F]FDG Biodistribution in Healthy Subjects [ Time Frame: 5 years ]
    We will use PET/MRI to establish the normal range of [18F]FDG uptake. (SUVmax) in various anatomic structures, such as the spinal cord, peripheral nerves, dorsal root ganglia, muscle, bones, joints, blood vessels, of asymptomatic subjects.

  2. 36 point Study Short-Form Health Survey [ Time Frame: 5 years ]
    Patient-reported state of health.

  3. Oswestry Disability Index [ Time Frame: 5 years ]
    Measure of disability, quality of life.

  4. Visual Analog Scale [ Time Frame: 5 years ]
    A visual, semi-quantitative method for patient-derived self-assessment of pain intensity.

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Age 18 years or older.
  • Chronic pain lasting greater than 2 months. For example: Low back pain, sciatica, complex regional pain syndrome, peripheral nerve injury, fibromyalgia, neuropathy, osteoarthritis, cancer pain, persistent post-operative pain, and migraine.
  • Provides informed consent
  • On a typical day, pain level of at least 4/10 on a 0-10 Comparative Pain Scale
  • Covid Vaccination status: Vaccinated or unvaccinated subjects who received a negative test result from the Covid test within 72 hours of the scan.

Exclusion Criteria:

  • MRI-incompatible
  • Diabetes
  • Pregnant or nursing
  • Non-English speaker
  • Claustrophobic

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03195270

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Contact: Sunyoung Park, BA 650-725-7668 sydoit@stanford.edu
Contact: Feliks Kogan, PhD fkogan@stanford.edu

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United States, California
Stanford University Recruiting
Stanford, California, United States, 94305
Contact: Sunyoung Park, BA       sydoit@stanford.edu   
Principal Investigator: Feliks Kogan, PhD         
Sponsors and Collaborators
Stanford University
GE Healthcare
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Principal Investigator: Feliks Kogan, PhD Assistant Professor of Radiology
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Feliks Kogan, Assistant Professor of Radiology, Stanford University
ClinicalTrials.gov Identifier: NCT03195270    
Other Study ID Numbers: IRB-24972
First Posted: June 22, 2017    Key Record Dates
Last Update Posted: November 3, 2022
Last Verified: October 2022
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: There is currently no plan to share the individual participant data with other researchers outside our group of researchers or referring physicians.

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
Keywords provided by Feliks Kogan, Stanford University:
Positron emission tomography
Magnetic Resonance Imaging
Chronic Pain
Neuropathic Pain
Inflammatory Pain
Nociceptive Pain
Additional relevant MeSH terms:
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Chronic Pain
Neurologic Manifestations
Fluorodeoxyglucose F18
Molecular Mechanisms of Pharmacological Action