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Clinical Trials/NCT02876874
NCT02876874
Unknown
Not Applicable

the Relationship Between the Activity of Rheumatoid Arthritis(RA) and Popliteal/Epitrochlear Lymph Node Morphology and the Drainage of Hand/Foot Superficial Lymphatic Vessels

Shanghai University of Traditional Chinese Medicine1 site in 1 country21 target enrollmentDecember 2014

Overview

Phase
Not Applicable
Intervention
indocyanine green(ICG)
Conditions
Rheumatoid Arthritis
Sponsor
Shanghai University of Traditional Chinese Medicine
Enrollment
21
Locations
1
Primary Endpoint
T-initial
Last Updated
9 years ago

Overview

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

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.

Registry
clinicaltrials.gov
Start Date
December 2014
End Date
December 2018
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Shanghai University of Traditional Chinese Medicine
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients fulfilling the classification criteria of American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) 2009 (scores more than 6 points)
  • Health participants normal in the test of blood/urine/stool routine, liver and kidney functions, electrocardiogram and without obvious medical history
  • Age 18 to 65 years
  • Fulling understood the whole trial and written informed consent.

Exclusion Criteria

  • Participants will be excluded when they combined with:
  • other types of autoimmune diseases such as ankylosing spondylitis, systemic lupus erythematosus, scleroderma, etc.,
  • lymphatic system disorders, such as lymphoma, lymphangitis and lymphatic edema due to lymphatic flow disorders,
  • disorders that effect the circulation of lymph or blood vessels such as hemangiomas,
  • tumors or cancer,
  • operation history within a year, such as joint orthopedics, tumor resection, etc.,
  • allergies or allergic to iodine, or radioactive iodine treatment within the last year,
  • with metal objects inside, such as pacemakers or nails,
  • the skin for the ultrasound inspection not intact such as eczema,ulceration, etc.,
  • lactation or pregnancy women or preparation to be pregnant within the next half year,

Arms & Interventions

the patients group

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

Intervention: indocyanine green(ICG)

the health group

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

Intervention: indocyanine green(ICG)

Outcomes

Primary Outcomes

T-initial

Time Frame: 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 Outcomes

  • lymphatic node transverse/longitudinal diameter ratio(the second day after enrollment)
  • T-max(after the injection of ICG, 1day after, 2 days after, 3 days after and 4days after)
  • S-max(after the injection of ICG, 1day after, 2 days after, 3 days after and 4days after)
  • %Clearance(after the injection of ICG, 1day after, 2 days after, 3 days after and 4days after)
  • Pulse(after the injection of ICG, 1day after, 2 days after, 3 days after and 4days after)
  • lymphatic node size(the second day after enrollment)
  • lymphatic node shape(the second day after enrollment)
  • lymphatic node types of edges(the second day after enrollment)
  • lymphatic node thickness of cortex/medulla(the second day after enrollment)
  • lymphatic node homogeneity(the second day after enrollment)
  • lymphatic node hilum(the second day after enrollment)
  • lymphatic node blood flow signal(the second day after enrollment)

Study Sites (1)

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