Study of the Relationship Between Body Composition, Insulin Resistance and HDL Levels
NCT ID: NCT02755818
Last Updated: 2021-02-23
Study Results
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View full resultsBasic Information
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TERMINATED
50 participants
OBSERVATIONAL
2008-10-22
2019-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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control
heparin at 50unit/kg of body weight having glomerular filtration rate (GFR) of greater than 60
Heparin
This is not an interventional study. The investigators use heparin at 50unit/kg of body weight to release enzyme lipoprotein lipase (LPL) from the body. LPL level will be used as part of calculation of lipid analysis and measurements
chronic renal disease (CKD3b)
heparin at 50unit/kg of body weight having glomerular filtration rate (GFR) of 30-45
Heparin
This is not an interventional study. The investigators use heparin at 50unit/kg of body weight to release enzyme lipoprotein lipase (LPL) from the body. LPL level will be used as part of calculation of lipid analysis and measurements
chronic renal disease (CKD4)
heparin at 50unit/kg of body weight having glomerular filtration rate (GFR) of 15-30
Heparin
This is not an interventional study. The investigators use heparin at 50unit/kg of body weight to release enzyme lipoprotein lipase (LPL) from the body. LPL level will be used as part of calculation of lipid analysis and measurements
chronic renal disease (CKD5)
heparin at 50unit/kg of body weight having glomerular filtration rate (GFR) of less than 15, or on hemodialysis
Heparin
This is not an interventional study. The investigators use heparin at 50unit/kg of body weight to release enzyme lipoprotein lipase (LPL) from the body. LPL level will be used as part of calculation of lipid analysis and measurements
Interventions
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Heparin
This is not an interventional study. The investigators use heparin at 50unit/kg of body weight to release enzyme lipoprotein lipase (LPL) from the body. LPL level will be used as part of calculation of lipid analysis and measurements
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* BMI 18-40 kg/m2; Hemodialysis dependent for at least 3 months, prevalent ESRD (end stage renal disease) cohort;
* GFR \> 15 \< 44 ml/min (CKD cohort);
* GFR \> 60 ml/min (Control cohort).
Exclusion Criteria
* Evidence of liver disorder, ie; hepatitis
* Evidence of thyroid disorders
* HIV by medical history (HIV test will not be performed)
* Renal transplant recipient
* Oral contraceptive/ hormone replacement therapy
* Systemic use of systemic or inhaled corticosteroids in the past month
* Contraindication to systemic anticoagulation (heparin administration is necessary to measure levels of LPL, HL);
* Hemoglobin \< 8.5 g/dl (anemia);
* Current, within 2 months use of any hypolipidemic or anti-diabetic agents;
* Patients treated with a fibric acid derivative or niacin in the past 4 weeks;
* Urinary protein excretion of greater than 0.5 grams per day;
* Any other condition that, in the opinion of the investigators, would put the subject at risk.
18 Years
75 Years
ALL
Yes
Sponsors
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Dialysis Clinic, Inc.
INDUSTRY
University of California, Davis
OTHER
Responsible Party
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Principal Investigators
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George A Kaysen, MD PhD
Role: PRINCIPAL_INVESTIGATOR
University of California, Davis
Tjien Dwyer, BS
Role: STUDY_DIRECTOR
University of California, Davis
References
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Molfino A, Don BR, Kaysen GA. Comparison of bioimpedance and dual-energy x-ray absorptiometry for measurement of fat mass in hemodialysis patients. Nephron Clin Pract. 2012;122(3-4):127-33. doi: 10.1159/000350817. Epub 2013 May 9.
Provided Documents
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Document Type: Informed Consent Form
Document Type: Study Protocol
Document Type: Statistical Analysis Plan
Study Documents
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Document Type: Informed Consent Form
for a copy of Approved Consent Form-please contact Study Coordinator -Tjien Dwyer at [email protected]
View DocumentRelated Links
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Nephron Clin Pract. 2012; 122(0): 127-133.
Other Identifiers
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220939
Identifier Type: -
Identifier Source: org_study_id
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