Kidney Precision Medicine Project (KPMP) - COVID-19 Protocol
NCT ID: NCT05384899
Last Updated: 2022-05-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
90 participants
OBSERVATIONAL
2021-06-15
2022-10-30
Brief Summary
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This joint protocol aims to synergize the COVID-19 study efforts of KPMP academic research centers, to collectively study COVID-19, including its renal presentation using kidney tissue and/or biofluids from patients suffering from COVID-19. This will increase the breadth and depth of data available to the public to expedite discoveries, identify therapeutics, and improve outcomes for patients with COVID-19. It will additionally bring the expertise of KPMP investigators to bear against this pandemic.
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Detailed Description
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Despite significant effort from industry and academia, development of pharmacologic therapies for AKI and CKD has been hampered by:
Non-predictive animal models The inability to identify and prioritize human targets The limited availability of human kidney biopsy tissue A poor understanding of AKI and CKD heterogeneity Historically, AKI and CKD have been described as single, uniform diseases. However, growing consensus suggests that different disease pathways lead to different subgroups of AKI and CKD (AKIs and CKDs).
Access to human kidney biopsy tissue is a critical first step to define disease heterogeneity and determine the precise molecular pathways that will facilitate identification of specific drug targets and ultimately enable individualized care for people with AKI and CKD.
A number of research centers across the United States are collaborating to bring state-of-the-art technologies together to:
Ethically obtain and evaluate kidney biopsies from participants with AKI or CKD Define disease subgroups Create a kidney tissue atlas Identify critical cells, pathways, and targets for novel therapies
The KPMP is made up of three distinct, but highly interactive, activity groups:
Recruitment Sites: The recruitment sites (RS) are responsible for recruiting participants with AKI or CKD into the longitudinal study and performing the kidney biopsy.
Tissue Interrogation Sites: The tissue interrogation sites (TIS) are responsible for developing and using innovative technologies to analyze the biopsy tissue.
Central Hub: The central hub is responsible for aggregating, analyzing, and visualizing the generated data and providing scientific, infrastructure, and administrative support for the KPMP consortium.
Since its inception, KPMP has developed sophisticated protocols for collection and analysis of human kidney tissue, and for collection of biofluids. Members of the consortium have wide-ranging expertise in conducting clinical studies, processing kidney tissue, advanced structural and molecular analysis and complex bioinformatics analysis, which will be used to to leverage effectively as a group to better understand kidney disease.
This joint protocol aims to synergize the COVID-19 study efforts of KPMP academic research centers, to collectively study COVID-19, including its renal presentation using kidney tissue and/or biofluids from patients suffering from COVID-19. This will increase the breadth and depth of data available to the public to expedite discoveries, identify therapeutics, and improve outcomes for patients with COVID-19. It will additionally bring the expertise of KPMP investigators to bear against this pandemic.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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COVID-19 Patients
The focus will be on patients with AKI in the setting of COVID-19 disease.
No interventions assigned to this group
Eligibility Criteria
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Exclusion Criteria
* Non-English or Spanish language
* Less than 18 years of age
* Severe allergy to iodinated contrast
* Transplant recipient (kidney or non-kidney, including solid organ and bone marrow transplantation)
* Additional vulnerable individuals (incarcerated, institutionalized, or otherwise unable to participate in the study)
* Inability to provide informed consent or obtain surrogate consent from a legally authorized representative (LAR)
* Unwilling to receive blood transfusion (if needed)
* Baseline eGFR less than 15 ml/min/m2
If known at the time of enrollment, or determined by kidney ultrasound before the biopsy procedure (may be the same day as the biopsy procedure)
* Kidney size less than 8 cm (percutaneous biopsies only)
* Solitary or single functioning kidney
* Evidence of urinary tract obstruction or hydronephrosis
* Multiple bilateral kidney cysts
18 Years
ALL
No
Sponsors
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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
NIH
University of Michigan
OTHER
Icahn School of Medicine at Mount Sinai
OTHER
Broad Institute of MIT and Harvard
OTHER
Indiana University
OTHER
Johns Hopkins University
OTHER
Joslin Diabetes Center
OTHER
Pacific Northwest National Laboratory
FED
Princeton University
OTHER
Stanford University
OTHER
Ohio State University
OTHER
University of California, San Diego
OTHER
University of California, San Francisco
OTHER
The University of Texas Health Science Center at San Antonio
OTHER
University of Texas
OTHER
Washington University School of Medicine
OTHER
Yale University
OTHER
Beth Israel Deaconess Medical Center
OTHER
University of Washington
OTHER
Responsible Party
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Jonathan Himmelfarb
Professor, School of Medicine
Principal Investigators
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Jonathan Himmelfarb, MD
Role: PRINCIPAL_INVESTIGATOR
University of Washington
Locations
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Yale University
New Haven, Connecticut, United States
Johns Hopkins University
Baltimore, Maryland, United States
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States
University of Texas at Southwestern
Dallas, Texas, United States
Countries
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Other Identifiers
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SITE00000750 (COV001)
Identifier Type: -
Identifier Source: org_study_id
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