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Completed No phase listed Observational

CRIC-Visceral Adiposity and Physical Fitness in Chronic Kidney Disease

ClinicalTrials.gov ID: NCT02405650

Public ClinicalTrials.gov record NCT02405650. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 15, 2026, 1:15 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Visceral Adiposity and Physical Fitness in CKD

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Obesity and chronic kidney disease (CKD) are major public health problems. In contrary to observations in general population, higher body mass index in those with pre-existing CKD is associated with lower mortality. Chronic Renal Insufficiency Cohort (CRIC) is an ongoing observational study to examine the consequences of CKD with a particular focus on cardiovascular illness like myocardial infarction (heart attack) and stroke. Among CRIC study participants, the investigators propose to obtain visceral and subcutaneous adiposity and physical fitness measures and study its associations with patient-centered outcomes. This study will help the investigators understand the independent and combined effects of visceral adiposity and physical fitness on cardiovascular disease, renal disease progression and death among those with CKD. Further, it will identify mechanisms that could be targeted to reduce the detrimental effects of visceral adiposity in those with kidney disease.

Study identification

NCT ID
NCT02405650
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Baylor College of Medicine
Other
Enrollment
453 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
21 Years to 79 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2015
Primary completion
Mar 30, 2018
Completion
Mar 30, 2018
Last update posted
Jul 21, 2019

2015 – 2018

United States locations

U.S. sites
10
U.S. states
6
U.S. cities
6
Facility City State ZIP Site status
University of Illinois at Chicago Chicago Illinois 60612
University of Maryland Medical System Baltimore Maryland 21201
Johns Hopkins University - ProHealth Baltimore Maryland 21207
University of Michigan Ann Arbor Michigan 48109
Case Western Reserve University Cleveland Ohio 44106
Metro Health Medical Center Cleveland Ohio 44109
Cleveland Clinic Cleveland Ohio 44195
University of Pennsylvania Scientific & Data Coordinating Center Philadelphia Pennsylvania 19104
University of Pennsylvania Philadelphia Pennsylvania 19104
Baylor College of Medicine Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02405650, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 21, 2019 · Synced Sep 15, 2026

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The complete protocol, eligibility criteria, and contact information for NCT02405650 live on ClinicalTrials.gov.

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