Actively Recruiting
KIDney Injury in Times of COVID-19 (KIDCOV)
Led by University of California, San Francisco · Updated on 2025-07-28
2000
Participants Needed
3
Research Sites
313 weeks
Total Duration
On this page
Sponsors
U
University of California, San Francisco
Lead Sponsor
R
Rush University Medical Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
There is an unmet need to evaluate the impact of sub-clinical/mild COVID19 disease in the outpatient setting on prevalent and incident renal injury, as this data is currently unavailable. To capture the diversity of race/ethnic risk and COVID19 related municipal shelter-in-place guidance, the investigators will enroll COVID19-negative and COVID19-positive samples balanced by race/ethnicity from 3 different states, California, Michigan, and Illinois. Study endpoints will be assayed from urine samples mailed to the study team at 2, 6, and 12 months after their date of PCR test, with no requirement for these individuals to leave their homes to participate.
CONDITIONS
Official Title
KIDney Injury in Times of COVID-19 (KIDCOV)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Result of PCR-based COVID-19 test conducted in the past 4 weeks posted in EMR of participating academic medical center
- Age 18 years or older at enrollment
- Race/ethnicity, sex, age, and phone and/or home/email address provided
You will not qualify if you...
- Failure to provide written informed consent to comply with the study protocol
- Hospitalization within 4 weeks after SARS-CoV-2 test
- History of kidney transplant
- History of dialysis
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
UCSF
San Francisco, California, United States, 94143
Actively Recruiting
2
Rush University
Chicago, Illinois, United States, 60612
Actively Recruiting
3
University of Michigan
Ann Arbor, Michigan, United States, 48109
Actively Recruiting
Research Team
M
Minnie Sarwal, M.D., Ph.D.
CONTACT
T
Tara Sigdel, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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