Actively Recruiting

Age: 18Years +
All Genders
ID06824714

Prediction of Risk of Vascular Structural Damage in Patients With Large Vessel Vasculitis Using PET/MRA Imaging

Led by Nanjing Medical University · Updated on 2025-02-13

150

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Large vessel vasculitis (LVV) causes inflammation in large blood vessels, which can lead to severe complications like aneurysm and stroke. Current imaging methods have difficulty detecting vessel wall inflammation, making it hard to decide the best time and type of treatment. This research aims to improve examination methods to better assess disease activity and guide treatment decisions using PET/MRA imaging. The study uses positron emission tomography and magnetic resonance imaging (PET/MRA) to assess vascular wall inflammation in patients with LVV. After initial clinical assessment, lab tests, and PET/MRA scans, clinicians will decide on drug treatments such as glucocorticoids, immunosuppressants, or targeted therapies. Patients will be followed for 12 months, with clinic visits every 1 to 2 months based on their condition, and PET/MRA reassessments at 6 and 12 months. Participants will undergo clinical evaluations, laboratory tests, and PET/MRA scans at the start and during follow-up visits to monitor vascular changes. The main outcome measured is vascular structural progression over 12 months, along with imaging measures like SUV max. The study tracks patient health and disease progression through regular assessments during the one-year period to improve understanding of LVV activity and treatment effects.

CONDITIONS

Brief Title

Prediction of Risk of Vascular Structural Damage in Patients With Large Vessel Vasculitis (LVV) Based on PET/MRA Image Evaluation System

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinically suspected or confirmed large vessel vasculitis (LVV) and willing to undergo PET/MRA
  • Willingness to comply with long-term follow-up
  • Signed informed consent form
Not Eligible

You will not qualify if you...

  • Presence of other serious cardiovascular or cerebrovascular diseases, malignant tumors, infectious diseases, or severe kidney failure
  • Severe mental disorders or claustrophobia preventing examination cooperation
  • Having metal implants such as pacemakers, artificial heart valves, vascular clamps, aneurysm clamps, cochlear implants, insulin pumps, metal plates, artificial joints, electronic or artificial eyes
  • Allergy to contrast medium
  • Pregnant or breastfeeding women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Baseline Assessment

Duration - 1 day

Participants complete baseline clinical assessment, laboratory tests, and PET/MRA imaging to evaluate vascular inflammation.

1 visit (in-person)

Monitoring

Duration - Up to 12 months

Participants are monitored with clinical assessments and laboratory tests every 1 to 2 months according to their specific conditions.

Visits every 1 to 2 months

Imaging Visits

Duration - 12 months

PET/MRA re-examinations are done at 6 and 12 months after treatment to assess vascular changes.

2 visits (at 6 and 12 months)

Trial Site Locations

Total: 1 location

1

Department of Rheumatology and Immunology, Jiangsu Province Hospital, Nanjing Medical University

Nanjing, Jiangsu, China, 210029

Actively Recruiting

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Research Team

R

Rui LIU, MD

Q

Qian ZHANG, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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