Purpose

Chronic kidney disease (CKD) affects approximately 26 million Americans and disproportionately manifests in specific race and ethnic groups. Patients burdened with CKD have significant morbidity and reduced life expectancy. In addition to excessive suffering and lost productivity, the cost of managing this epidemic has reached $40 billion annually. The recognition that CKD is a major public health problem is reflected in the fourteen objectives outlined in Healthy People 2020 to begin to address the disease burden. Advancement in approaches to halt CKD progression has been slow despite growing global awareness of disease burden. 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, at the institutions of University of Michigan Health System, St. John Hospital, Wayne State University in Michigan, John H. Stroger Hospital in Illinois, Temple University Health System in Pennsylvania, and Levine Children's Hospital in North Carolina. This mechanism will feed the other Cores and provide biomedical investigators with approved projects the access to a dynamic pool of well characterized high risk kidney disease patients and their biological specimens to conduct high caliber translational research.

Conditions

Eligibility

Eligible Ages
All ages
Eligible Sex
All
Accepts Healthy Volunteers
Yes

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 - adults who have polycystic kidney disease - institutionalized persons - people currently participating in a blinded interventional clinical trial

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Chronic Kidney Disease Cohort chronic kidney disease patients with any type of kidney disease
Matched Control Group Healthy controls
Trios First degree relatives of pediatric chronic kidney disease cohort members

Recruiting Locations

University of Michigan Health System
Ann Arbor, Michigan 48109
Contact:
Chrysta Lienczewski
734-615-5021
boridly@med.umich.edu

More Details

NCT ID
NCT01016613
Status
Recruiting
Sponsor
University of Michigan

Study Contact

Chrysta Lienczewski
734-615-5021
boridley@med.umich.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.