Clinical Trials Directory

Trials / Completed

CompletedNCT01881295

Bioavailability of Potassium From Potatoes and Potassium Gluconate

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
45 (actual)
Sponsor
Purdue University · Academic / Other
Sex
All
Age
20 Years – 60 Years
Healthy volunteers
Accepted

Summary

This study is designed to compare the effect of sources of potassium on uptake and the effect of potassium on blood pressure.

Detailed description

The study will compare uptake of potassium from three different doses and sources; supplements (720, 1440 and 2160 mg) potatoes (720, 1440 and 2160 mg) or French fries (2160 mg). During 9 phases, participants will consume a controlled diet with the supplements, potato or french fries (every other week for 5 days). On the 4th day, blood and urine samples will be taken to monitor potassium uptake and excretion. Measures of blood pressure will be analyzed at defined time points throughout the intervention.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPlacebo control
DIETARY_SUPPLEMENTLow dose potassium gluconate
DIETARY_SUPPLEMENTMedium dose potassium gluconate
DIETARY_SUPPLEMENTHigh dose potassium gluconate
DIETARY_SUPPLEMENTLow dose potato
DIETARY_SUPPLEMENTMedium dose potato
DIETARY_SUPPLEMENTHigh dose potato
DIETARY_SUPPLEMENTHigh dose French fries
DIETARY_SUPPLEMENTBasal diet control

Timeline

Start date
2013-03-01
Primary completion
2014-08-01
Completion
2014-12-01
First posted
2013-06-19
Last updated
2018-05-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01881295. Inclusion in this directory is not an endorsement.