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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00244790
Other study ID # 0309-03
Secondary ID K23RR019615-01A1
Status Completed
Phase N/A
First received October 25, 2005
Last updated August 26, 2015
Start date April 2004
Est. completion date April 2014

Study information

Verified date August 2015
Source Indiana University
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if being overweight and eating lots of protein causes separate changes in the kidney that lead to kidney disease over time. These questions are important because the number of people who have kidney disease is quickly growing. If being overweight and eating lots of protein is found to cause kidney disease, then doctors may be able to limit the number of people with kidney disease by recommending weight loss and eating less protein


Description:

The purpose of this study is to test the hypothesis that being obese leads to changes in kidney function that are independent of, and enhanced by, high dietary protein intake. Kidney function will be measured by the kidney's ability to filter blood and by the amount of protein in the urine. The hypothesis will be tested in the following manner: The first part of the study will involve a crossover design comparing kidney function in obese people with stable weights on a low and high protein diet ("Low/High Protein Study"). The second part of the study will compare kidney function in obese people before and after weight reduction surgery ("Before/After Surgery Study"). Since certain changes in kidney function may lead to kidney disease over time, it is important to confirm the effects of obesity and dietary protein intake on the kidney, especially with the current rise in obese people and the popularity of high protein diets.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date April 2014
Est. primary completion date April 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Greater than 18 years of age

- Ability to give informed consent

- Not pregnant and using appropriate contraceptive methods, or not of childbearing potential

- BMI of 30 or higher

Exclusion Criteria:

- Iodine or shellfish allergy

- History of adverse reaction to intravenous contrast

- Dialysis dependence

- Diagnosis of diabetes mellitus or taking medicine for diabetes mellitus

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Behavioral:
Diet
crossover low vs high protein diet before and after weight loss

Locations

Country Name City State
United States University Hospital Indianapolis Indiana

Sponsors (2)

Lead Sponsor Collaborator
Indiana University School of Medicine National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary glomerular filtration rate days No
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