Clinical TrialID 735
Bioavailability of Potassium From Potatoes and Potassium Gluconate
NCT01881295
Potassium Bioavailability|Blood Pressure
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 735
- Evidence Id
- 735
- Core Evidence Id
- 735
- Source Clinical Trial Id
- 720
- Herb2 Clinical Trial Id
- HBCT000720
- Nct Id
- NCT01881295
- Title
- Bioavailability of Potassium From Potatoes and Potassium Gluconate
- Status
- Completed
- Phase
- Study Result
- No
- Study Condition
- Potassium Bioavailability|Blood Pressure
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: SINGLE (PARTICIPANT)|Primary Purpose: OTHER
- Intervention
- DIETARY_SUPPLEMENT: Placebo control|DIETARY_SUPPLEMENT: Low dose potassium gluconate|DIETARY_SUPPLEMENT: Medium dose potassium gluconate|DIETARY_SUPPLEMENT: High dose potassium gluconate|DIETARY_SUPPLEMENT: Low dose potato|DIETARY_SUPPLEMENT: Medium dose potato|DIETARY_SUPPLEMENT: High dose potato|DIETARY_SUPPLEMENT: High dose French fries|DIETARY_SUPPLEMENT: Basal diet control
- Intervention Allocation
- Randomized
- Intervention Model
- Crossover
- Intervention Mask
- Single
- Intervention Purpose
- Other
- Gender
- All
- Age
- Adult
- Enrollment
- 45
- Outcome Measure
- Bioavailability of Potassium, After 4 days of acclimation to the supplementation, absorption of potassium will be measured., 5 days
- Sponsor Collaborator
- Purdue University|Alliance for Potato Research and Education
- Funded By
- OTHER
- Location
- Purdue University, West Lafayette, Indiana, 47907, United States
- Other Id
- 1301013174
- Start Date
- 2013-03-01
- Primary Completion Date
- 2014-08
- Completion Date
- 2014-12
- First Posted
- 2013-06-19
- Results First Posted
- Last Update Posted
- 2018-05-09
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT01881295
- Title Cn
- Title En
- Bioavailability of Potassium From Potatoes and Potassium Gluconate
- Bilingual Status
- semi_complete