View Clinical Trial (Medical Research Study)
Sleep Disturbance as a Non-Traditional Risk Factor in CKD
| City: |
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Chicago |
| State: |
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Illinois |
| Zip Code: |
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60637 |
| Conditions: |
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Chronic Kidney Disease |
| Purpose: |
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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.
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| Study Summary: |
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| Criteria: |
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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
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| NCT ID: |
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NCT00817427 |
| Primary Contact: |
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Principal Investigator Eve Van Cauter, PhD University of Chicago
Annette Miller, RN, MSN Phone: 773-834-8871 Email: amiller@medicine.bsd.uchicago.edu
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| Backup Contact: |
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N/A |
| Location Contact: |
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Chicago, Illinois 60637 United States
There is no listed contact information for this specific location.
Site Status: Recruiting |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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May 22, 2013 |
| Modifications to this listing: |
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