Relationship Between the Activity of Rheumatoid Arthritis and Lymph Node Morphology and Lymphatics Drainage

Sponsor
Shanghai University of Traditional Chinese Medicine (Other)
Overall Status
Unknown status
CT.gov ID
NCT02876874
Collaborator
(none)
21
2
48
10.5
0.2

Study Details

Study Description

Brief Summary

To observe the relationship between the activity of rheumatoid arthritis and popliteal/epitrochlear lymph node morphology and the drainage of hand/foot superficial lymphatic vessels

Condition or Disease Intervention/Treatment Phase
  • Drug: indocyanine green(ICG)

Detailed Description

Rheumatoid Arthritis patients and health participants will be recruited in our research. Then the classification of American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) 2009 will be used to identify rheumatoid arthritis patients. The measurement of disease activity are Disease Activity Score 28 (DAS28) combined with the synovitis, bone edema and bone erosion of hand and wrist detected by magnetic resonance (MR) and Doppler ultrasound (DUS).The morphology of lymph node in popliteal/epitrochlear are scanned by 3-dimensional MR and DUS. The drainage of hand/foot superficial lymphatic vessels are detected in sight of near infrared ray (NIR) with the applying of Indocyanine Green (ICG) subcutaneously. We'll conduct correlation analysis to reveal the relationship between the activity of Rheumatoid Arthritis and lymph nodes morphology and lymphatic vessels drainage.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
21 participants
Time Perspective:
Prospective
Official Title:
the Relationship Between the Activity of Rheumatoid Arthritis(RA) and Popliteal/Epitrochlear Lymph Node Morphology and the Drainage of Hand/Foot Superficial Lymphatic Vessels
Study Start Date :
Dec 1, 2014
Anticipated Primary Completion Date :
Dec 1, 2017
Anticipated Study Completion Date :
Dec 1, 2018

Arms and Interventions

Arm Intervention/Treatment
the patients group

0.1ml, 5mg/ml indocyanine green(ICG) will be injected subcutaneously to aid visualization in NIR

Drug: indocyanine green(ICG)
ICG will be injected into the dorsal of hand/foot
Other Names:
  • IC-GREEN®(indocyanine green for injection,USP),AKORN,Inc
  • the health group

    0.1ml, 5mg/ml indocyanine green(ICG) will be injected subcutaneously to aid visualization in NIR

    Drug: indocyanine green(ICG)
    ICG will be injected into the dorsal of hand/foot
    Other Names:
  • IC-GREEN®(indocyanine green for injection,USP),AKORN,Inc
  • Outcome Measures

    Primary Outcome Measures

    1. T-initial [after the injection of ICG from the first day to the fourth day after]

      the time that it takes for the ICG to be detected in vessels

    Secondary Outcome Measures

    1. S-max [after the injection of ICG, 1day after, 2 days after, 3 days after and 4days after]

      the maximum ICG signal intensity observed in the target lymph node during the first day imaging session

    2. T-max [after the injection of ICG, 1day after, 2 days after, 3 days after and 4days after]

      the time it takes for a nodes in cubital fossa or popliteal space to achieve maximal ICG signal intensity

    3. %Clearance [after the injection of ICG, 1day after, 2 days after, 3 days after and 4days after]

      an assessment of ICG wash out through the lymphatics and is quantified as the percent difference of ICG signal intensity between the two ICG-NIR images from a certain region at a) S-max (first day) and b) 24 hours post ICG injection,

    4. Pulse [after the injection of ICG, 1day after, 2 days after, 3 days after and 4days after]

      ICG pulses that pass the a certain region within 400 seconds.

    5. lymphatic node size [the second day after enrollment]

    6. lymphatic node shape [the second day after enrollment]

    7. lymphatic node transverse/longitudinal diameter ratio [the second day after enrollment]

    8. lymphatic node types of edges [the second day after enrollment]

    9. lymphatic node thickness of cortex/medulla [the second day after enrollment]

    10. lymphatic node homogeneity [the second day after enrollment]

    11. lymphatic node hilum [the second day after enrollment]

    12. lymphatic node blood flow signal [the second day after enrollment]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. Patients fulfilling the classification criteria of American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) 2009 (scores more than 6 points)

    2. Health participants normal in the test of blood/urine/stool routine, liver and kidney functions, electrocardiogram and without obvious medical history

    3. Age 18 to 65 years

    4. Fulling understood the whole trial and written informed consent.

    Exclusion Criteria:
    Participants will be excluded when they combined with:
    1. other types of autoimmune diseases such as ankylosing spondylitis, systemic lupus erythematosus, scleroderma, etc.,

    2. lymphatic system disorders, such as lymphoma, lymphangitis and lymphatic edema due to lymphatic flow disorders,

    3. disorders that effect the circulation of lymph or blood vessels such as hemangiomas,

    4. tumors or cancer,

    5. operation history within a year, such as joint orthopedics, tumor resection, etc.,

    6. allergies or allergic to iodine, or radioactive iodine treatment within the last year,

    7. with metal objects inside, such as pacemakers or nails,

    8. the skin for the ultrasound inspection not intact such as eczema,ulceration, etc.,

    9. lactation or pregnancy women or preparation to be pregnant within the next half year,

    10. without whole limbs to inspect,

    11. mania, depression or other mental disorder

    12. medical disorders such as diabetes, hypertension or hyperlipidemia, etc.,

    13. a history of infectious diseases such as tuberculosis, hepatitis B or HIV, etc.,

    14. a history of drug abuse such as opioid analgesics, sedative-hypnotics or alcohol abuse, etc.,

    15. severe liver or kidney dysfunction (Alanine Aminotransferase(ALT) or Aspartate Aminotransferase(AST) two times higher than the upper limit of normal, serum creatinine levels more than two times the upper limit of normal);

    16. poor compliance.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Longhua Hospital, Shanghai University of TCM Shanghai Shanghai China 200032
    2 Longhua Hospital, Shanghai University of TCM Shanghai China 200032

    Sponsors and Collaborators

    • Shanghai University of Traditional Chinese Medicine

    Investigators

    • Principal Investigator: Yong-jun Wang, Dr., Longhua Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Shanghai University of Traditional Chinese Medicine
    ClinicalTrials.gov Identifier:
    NCT02876874
    Other Study ID Numbers:
    • RA and lymphatic vessels
    First Posted:
    Aug 24, 2016
    Last Update Posted:
    Aug 24, 2016
    Last Verified:
    Aug 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Shanghai University of Traditional Chinese Medicine
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 24, 2016