Clinical Phenotyping Resource and Biobank Core of the Michigan O'Brien Renal Center (C-PROBE)
Recruitment status was Recruiting
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Purpose
More than 10 million Americans have chronic kidney disease and every year, approximately 100,000 new patients develop end stage renal disease (ESRD) resulting in incalculable human suffering, a high rate of premature mortality, catastrophic physical and emotional disability and prohibitive costs to the U.S. health care system. The current medical therapies for chronic kidney disease, which disproportionately affect African Americans and other minority groups and account for 70% of ESRD, cases are woefully inadequate. This O'Brien Kidney Research Core will create opportunities for novel insights through characterization of tissue profiles that will define new disease markers and molecular pathways and will be available to all kidney investigators on the www. It will thereby fundamentally alter the starting point for research into prevention of progression of these kidney diseases. C-PROBE is an essential element of the center grant and presents a biomedical resource core consisting of: (1) clinical phenotyping (that is, systematic identification of observable physical and biomedical characteristics) of kidney disease patients including the accurate measurement of kidney function; and (2) a specimen BioBank which will store blood, urine and kidney tissue samples . A key component of C-PROBE is therefore that it contains a proven mechanism to collect samples from high risk groups including minorities, that will feed the other Cores and provide biomedical investigators at the institutions of University of Michigan Health System, St. John Hospital, Wayne State University in Michigan and University of Illinois in Chicago access to a dynamic pool of well characterized high risk kidney disease patients and their biological specimens to conduct high caliber translational research.
| Condition |
|---|
|
Chronic Kidney Disease Glomerulopathy |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Clinical Phenotyping Resource and Biobank Core of the Michigan O'Brien Renal Center |
Urine, blood and renal tissue, if available
| Estimated Enrollment: | 1500 |
| Study Start Date: | January 2009 |
| Groups/Cohorts |
|---|
| Chronic Kidney Disease Cohort |
| Matched Control Group |
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Nephrology clinic patients and community members
Inclusion Criteria:
- persons of any age who have chronic kidney disease (abnormally high protein in urine or reduced kidney function determined by blood tests)
- a small number of people without chronic kidney disease
Exclusion Criteria:
- people on hemodialysis or peritoneal dialysis
- people who have had a kidney transplant
- people unable or unwilling to provide consent
- women who are pregnant or nursing
- people who have polycystic kidney disease
- people with a hemoglobin of <9 at the time of enrollment
- institutionalized persons
- people currently participating in a blinded interventional clinical trial
Contacts and Locations| United States, Illinois | |
| University of Illinois at Chicago | Recruiting |
| Chicago, Illinois, United States, 60612 | |
| Contact: Alberto Cabrales 312-996-2937 acabrals@uic.edu | |
| Principal Investigator: Kalyani Perumal, MD | |
| United States, Michigan | |
| University of Michigan Health System | Recruiting |
| Ann Arbor, Michigan, United States, 48109 | |
| Contact: Jennifer J Hawkins, MPH 734-615-8304 jenjoyce@med.umich.edu | |
| Contact: Chrysta Lienczewski, BS 734-615-5021 boridley@med.umich.edu | |
| Principal Investigator: Crystal A Gadegbeku, MD | |
| St. John's Health System | Recruiting |
| Detroit, Michigan, United States, 48236 | |
| Contact: Sherry Gasko, RN, BSN 313-886-8787 ext 1264 Sherry.Gasko@stjohn.org | |
| Contact: Tina Cavendish 313-886-8787 ext 1266 tcavendish@scsp.net | |
| Principal Investigator: Susan Steigerwalt, MD | |
| Wayne State University | Recruiting |
| Detroit, Michigan, United States, 48201 | |
| Contact: Carol Muzyk, CCRP 313-745-2378 cmuzyk@med.wayne.edu | |
| Principal Investigator: Kalyani Mehta, MD | |
| Principal Investigator: | Frank C Brosius, MD | University of Michigan |
| Study Director: | Crystal A Gadegbeku, MD | University of Michigan Health System |
| Study Director: | Matthias Kretzler, MD | University of Michigan Health System |
More Information
No publications provided
| Responsible Party: | Frank Brosius, MD, University of Michigan Health Systems |
| ClinicalTrials.gov Identifier: | NCT01016613 History of Changes |
| Other Study ID Numbers: | P30 DK 081943 |
| Study First Received: | November 18, 2009 |
| Last Updated: | April 7, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of Michigan:
|
chronic kidney disease glomerulonephritis proteinuria |
nephrotic syndrome nephropathy biobank |
Additional relevant MeSH terms:
|
Kidney Diseases Renal Insufficiency, Chronic Kidney Failure, Chronic Urologic Diseases Renal Insufficiency |
ClinicalTrials.gov processed this record on May 19, 2013