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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RECRUITING
2000 participants
OBSERVATIONAL
2021-03-01
2027-03-31
Brief Summary
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Detailed Description
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Early detection of new or worsening kidney injury is urgently needed in order to implement preventative measures and target therapeutics that can minimize excess post-COVID19 kidney damage. A complete and standardized understanding of the trajectory and risk factors for kidney injury associated with COVID19+ disease is critical to informing the design and implementation of preventative and therapeutic strategies for COVID19-mediated kidney injury.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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COVID-19 Negative
Control group to measure progression of AKI/kidney injury overtime
Urine Collection
A urine collection kit will be mailed to subjects' residence at 3 different timepoints over the course of 1 year to be returned to study team, upon which KIT score and other biomarkers will be assessed as outlined in the study design.
COVID-19 Positive
Study group to assess AKI trajectory/progression and associated risk factors of kidney injury with SARS-CoV-2 infection
Urine Collection
A urine collection kit will be mailed to subjects' residence at 3 different timepoints over the course of 1 year to be returned to study team, upon which KIT score and other biomarkers will be assessed as outlined in the study design.
Interventions
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Urine Collection
A urine collection kit will be mailed to subjects' residence at 3 different timepoints over the course of 1 year to be returned to study team, upon which KIT score and other biomarkers will be assessed as outlined in the study design.
Eligibility Criteria
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Inclusion Criteria
* Age 18 years or older at enrollment
* Race/ethnicity, sex, age, and phone and/or home/email address provided
Exclusion Criteria
* Hospitalization up to 4 weeks after SARS-CoV-2 test
* History of kidney transplant
* History of dialysis
18 Years
ALL
Yes
Sponsors
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Rush University Medical Center
OTHER
University of Michigan
OTHER
University of California
OTHER
University of California, San Francisco
OTHER
Responsible Party
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Principal Investigators
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Minnie Sarwal, M.D., Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University of California, San Francisco
Locations
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UCSF
San Francisco, California, United States
Rush University
Chicago, Illinois, United States
University of Michigan
Ann Arbor, Michigan, United States
Countries
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Central Contacts
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Facility Contacts
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BS
Role: backup
References
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Other Identifiers
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KIDCOV2020
Identifier Type: -
Identifier Source: org_study_id
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