- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00381277
The Effects of Sports Drinks on Urinary Lithogenicity
February 18, 2011 updated by: VA New York Harbor Healthcare System
The effect of sports drinks on the tendency to form kidney stones has not been assessed.
Patients will drink 1 liter a day of 2 sports drinks and collect urine to determine changes in urine chemistry that may decrease the risk of forming stones.
Study Overview
Detailed Description
Participants will drink 1 liter of water each day for one week in the control period, then 1 liter of sports drink each day for one week during the experimental period.
Urine collections will be performed during both periods.
Diet will be chosen by participants and a food diary will be kept so that participants can replicate diet during the urine collections.
Study Type
Interventional
Enrollment
10
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
New York, New York, United States, 10010
- New York Harbor VAMC
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- age 18-80 years old
- men and women
- able to sign informed consent
Exclusion Criteria:
- history of kidney stones
- bone disease
- parathyroid disease
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
---|
Urinary supersaturation of calcium oxalate
|
Urinary citrate excretion
|
Urinary calcium excretion
|
Urinary sodium excretion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: David S Goldfarb, MD, New York Harbor VAMC
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2006
Primary Completion (Actual)
March 1, 2006
Study Completion (Actual)
September 1, 2006
Study Registration Dates
First Submitted
September 26, 2006
First Submitted That Met QC Criteria
September 26, 2006
First Posted (Estimate)
September 27, 2006
Study Record Updates
Last Update Posted (Estimate)
February 21, 2011
Last Update Submitted That Met QC Criteria
February 18, 2011
Last Verified
February 1, 2011
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- DG-1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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