Clinical Phenotyping Resource and Biobank Core of the Michigan O'Brien Renal Center

Status: Recruiting
Location: See all (5) locations...
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: t
View:

• 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

Locations
United States
Michigan
University of Michigan Health System
RECRUITING
Ann Arbor
St. John's Health System
COMPLETED
Detroit
Wayne State University
COMPLETED
Detroit
North Carolina
Levine Children's Hospital
COMPLETED
Charlotte
Pennsylvania
Temple University
COMPLETED
Philadelphia
Contact Information
Primary
Chrysta Lienczewski
boridley@med.umich.edu
734-615-5021
Backup
Markus Bitzer, MD
markusbi@med.umich.edu
734-763-4688
Time Frame
Start Date: 2009-01
Estimated Completion Date: 2030-07
Participants
Target number of participants: 1800
Treatments
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
Related Therapeutic Areas
Sponsors
Collaborators: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Temple University, St. John Health System, Michigan
Leads: University of Michigan

This content was sourced from clinicaltrials.gov