- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03180021
Dynamic Imaging of Variation in Lupus Nephritis (DIVINE)
Study Overview
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Colorado
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Aurora, Colorado, United States, 80045
- The Regents of the University of Colorado
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New York
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New York, New York, United States, 10032
- The Trustees of Columbia University in the City of New York
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New York, New York, United States, 10002
- New York University School of Medicine
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Ohio
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Columbus, Ohio, United States, 43210
- Ohio State University
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South Carolina
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Charleston, South Carolina, United States, 29425
- Medical University of South Carolina
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Texas
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Dallas, Texas, United States, 75390
- University of Texas Southwestern Medical Center
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Provide written informed consent agreeing to all study procedures, before any study- specific procedures are done.
- Male and female subjects 18 to 65 years of age, inclusive.
- Subjects currently being evaluated for new or recurrent LN with a SOC kidney biopsy planned OR being evaluated for IgA nephropathy and with a SOC kidney biopsy planned.
- Patients with LN must meet American College of Rheumatology (ACR) or Systemic Lupus Collaborating Clinics (SLICC) criteria for Systemic Lupus Erythematosus (SLE).
- Subjects with a life expectancy >6 months.
Exclusion Criteria:
- Participation in another investigational study during same time period.
- Contraindication to receiving a GBCA.
- More than 2 previous lifetime exposures to a GBCA.
- Any contraindication to MRI, including metal implants, claustrophobia or morbid obesity.
- Acute or chronic severe renal insufficiency (glomerular filtration rate [GFR] <40 mL per minute per 1.73 m2).
- Subject requiring dialysis.
- Presence of pre-existing renal disease unrelated to SLE or IgA nephropathy, respectively.
- Acute renal insufficiency of any severity caused by the hepato-renal syndrome.
- Previous or pre-existing nephrogenic systemic fibrosis.
- History of clinically significant anti-phospholipid syndrome.
- Chronic liver function impairment, indicated by liver function tests (aspartate aminotransferase [AST], alanine aminotransferase [ALT]) >2-fold upper limit of normal.
- Platelet count <50,000/μL.
- Hemoglobin <8.0 g/dL.
- History of or presence of central nervous system (CNS) disease such as active lupus cerebritis or multiple sclerosis that might compromise blood brain barrier function.
- Infection that is clinically relevant, particularly hepatitis B virus (HBV), hepatitis C virus (HCV) and/or human immunodeficiency virus (HIV).
- Pregnant or nursing females, or females not using effective contraception.
- Inability or unwillingness to return to the research site clinic for study visits at baseline and at 6 months.
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Patients with Lupus Nephritis
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This is a multicenter, non-interventional, pilot study. Eligible subjects will have a baseline MRI of the kidney, including anatomical, DWI, BOLD, T1rho, and DCE-MRI, utilizing a macrocyclic gadolinium-based contrast agent (GBCA), followed by planned standard of care (SOC) renal biopsy and clinical laboratory assessments. Additional serum and urine will be collected from subjects at baseline for analysis of research biomarkers. Following the results of the biopsy and clinical laboratory assessments, subjects will be treated for their underlying disease at the discretion of the investigator. At 6 months, subjects will return to the clinic for a second MRI, SOC clinical and laboratory evaluation and collection of serum and urine for analysis of research biomarkers. |
|
Patients with IgA Neuropathy
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This is a multicenter, non-interventional, pilot study. Eligible subjects will have a baseline MRI of the kidney, including anatomical, DWI, BOLD, T1rho, and DCE-MRI, utilizing a macrocyclic gadolinium-based contrast agent (GBCA), followed by planned standard of care (SOC) renal biopsy and clinical laboratory assessments. Additional serum and urine will be collected from subjects at baseline for analysis of research biomarkers. Following the results of the biopsy and clinical laboratory assessments, subjects will be treated for their underlying disease at the discretion of the investigator. At 6 months, subjects will return to the clinic for a second MRI, SOC clinical and laboratory evaluation and collection of serum and urine for analysis of research biomarkers. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Diffusion Weight Imaging
Time Frame: 7 Months
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Diffusion weighted imaging (DWI) measures ADC values that quantify the combined effects of blood microcirculation and Brownian motion of water molecules within the interstitial space.
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7 Months
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Blood Oxygen Level Dependent Imaging
Time Frame: 7 Months
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Blood oxygen level dependent (BOLD) imaging has been widely used to analyze blood flow in various 15 and is the preferred method to detect regional differences in blood flow.
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7 Months
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T1rho Imaging
Time Frame: 7 Months
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T1rho (T1rho) imaging is an MRI technique that is sensitive to the presence of macromolecules, such as collagen and proteoglycan 13.
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7 Months
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Dynamic Contrast Enhanced Magnetic Resonance Imaging
Time Frame: 7 Months
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Dynamic contrast enhanced (DCE) MRI (DCE-MRI) is an imaging method where T1-weighted MRI scans are acquired dynamically after injection of an MRI contrast agent (e.g., macrocylic gadolinium).
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7 Months
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RIL-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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