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View Clinical Trial (Medical Research Study)


Sleep Disturbance as a Non-Traditional Risk Factor in CKD

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City:   Chicago
State:   Illinois
Zip Code:   60637
Conditions:   Chronic Kidney Disease
Purpose:   This study is designed to determine if either short night time sleep or poor night time sleep could be a risk factor for increasing the rate at which kidney function deteriorates in persons with mild to moderate kidney disease.
Study Summary:  
Criteria:   Inclusion Criteria: - Mild to Moderate CKD - Healthy controls age and gender matched to CKD subjects - Regular bedtimes of at least 6h/night, sedentary lifestyle Exclusion Criteria: - Diabetes - Current or previous dialysis for more than 1 month - Uncontrolled hypertension - Heart failure - Liver disease - HIV - Hemoglobin < 10.5 g/dl - Treatment with EProcrit, Epogen, or Aranesp - Bone or organ transplant, - Use of immunosuppressive drugs within past 6 months - Current oral contraceptive use - Current pregnancy - Chemotherapy for malignancy within past 2 years
NCT ID:   NCT00817427
Primary Contact:   Principal Investigator
Eve Van Cauter, PhD
University of Chicago

Annette Miller, RN, MSN
Phone: 773-834-8871
Email: amiller@medicine.bsd.uchicago.edu
Backup Contact:   N/A
Location Contact:   Chicago, Illinois 60637
United States



There is no listed contact information for this specific location.

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 22, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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