Clinical TrialID 8401
The Potassium Supplementation Study
NCT05887622
Cardiovascular Health|Cardiovascular Risk Factor
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 8401
- Evidence Id
- 8401
- Core Evidence Id
- 8401
- Source Clinical Trial Id
- 8399
- Herb2 Clinical Trial Id
- HBCT008399
- Nct Id
- NCT05887622
- Title
- The Potassium Supplementation Study
- Status
- Recruiting
- Phase
- Study Result
- No
- Study Condition
- Cardiovascular Health|Cardiovascular Risk Factor
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: SINGLE (PARTICIPANT)|Primary Purpose: PREVENTION
- Intervention
- DIETARY_SUPPLEMENT: Potassium chloride supplement|DIETARY_SUPPLEMENT: Placebo
- Intervention Allocation
- Randomized
- Intervention Model
- Crossover
- Intervention Mask
- Single
- Intervention Purpose
- Prevention
- Gender
- All
- Age
- Adult
- Enrollment
- 30
- Outcome Measure
- Conduit artery endothelial dependent dilation, The difference in flow-mediated dilation (FMD) between the 3 diets, on day 10 of each diet|Blood pressure reactivity, The change in both systolic and diastolic blood pressure during handgrip exercise and cold pressor test from baseline, on day 10 of each diet|Superoxide levels, The difference in superoxide levels as measured by electronic paramagnetic resonance (EPR) between the 3 diets will be assessed, on day 10 of each diet
- Sponsor Collaborator
- University of Delaware
- Funded By
- OTHER
- Location
- Tower at STAR, Newark, Delaware, 19713, United States
- Other Id
- 1465208
- Start Date
- 2022-01-24
- Primary Completion Date
- 2025-01-31
- Completion Date
- 2025-06-30
- First Posted
- 2023-06-05
- Results First Posted
- Last Update Posted
- 2023-06-05
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT05887622
- Title Cn
- Title En
- The Potassium Supplementation Study
- Bilingual Status
- semi_complete