2009
DOI: 10.2215/cjn.00070109
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Chronic Renal Insufficiency Cohort (CRIC) Study

Abstract: Background and objectives: The Chronic Renal Insufficiency Cohort (CRIC) Study was established to examine risk factorsfor the progression of chronic kidney disease (CKD) and cardiovascular disease (CVD) in patients with CKD. We examined baseline demographic and clinical characteristics.Design, setting, participants, & measurements: Seven clinical centers recruited adults who were aged 21 to 74 yr and had CKD using age-based estimated GFR (eGFR) inclusion criteria. At baseline, blood and urine specimens were co… Show more

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Cited by 517 publications
(474 citation statements)
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“…The study design and baseline characteristics of participants have been described previously (17,18). The study protocol was approved by the institutional review board of each participating site; written informed consent was obtained from all participants.…”
Section: Methodsmentioning
confidence: 99%
“…The study design and baseline characteristics of participants have been described previously (17,18). The study protocol was approved by the institutional review board of each participating site; written informed consent was obtained from all participants.…”
Section: Methodsmentioning
confidence: 99%
“…The design, methods, and baseline characteristics of the Chronic Renal Insufficiency Cohort (CRIC) study population have been published (18,19). Briefly, CRIC is a prospective observational study of patients with mild-to-moderate kidney disease that was established by the National Institute of Diabetes and Digestive and Kidney Diseases to examine risk factors for kidney and cardiovascular disease progression in CKD.…”
Section: Methodsmentioning
confidence: 99%
“…[15][16][17] The CRIC Study recruited 3939 adults from May 2003 to June 2008, aged 21-74 years, with mild to moderate CKD from general medicine and specialty clinics at seven clinical centers across the U.S. (Ann Arbor, Michigan; Baltimore, Maryland; Chicago, Illinois; Cleveland, Ohio; New Orleans, Louisiana; Philadelphia, Pennsylvania; and Oakland, California). Participants were followed with annual in-clinic visits and interim telephone contact.…”
Section: Study Populationmentioning
confidence: 99%
“…Exclusion criteria included inability to consent, institutionalization, pregnancy, and certain chronic conditions. [15][16][17] The study protocol was approved by Institutional Review Boards of participating centers and is in accordance with the principles of the Declaration of Helsinki. All study participants provided written informed consent.…”
Section: Study Populationmentioning
confidence: 99%
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