Clinical TrialID 8400
Potassium Intake-response Trial to Control Hypertension
NCT05758142
Blood Pressure
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 8400
- Evidence Id
- 8400
- Core Evidence Id
- 8400
- Source Clinical Trial Id
- 8398
- Herb2 Clinical Trial Id
- HBCT008398
- Nct Id
- NCT05758142
- Title
- Potassium Intake-response Trial to Control Hypertension
- Status
- Terminated
- Phase
- Study Result
- No
- Study Condition
- Blood Pressure
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: TRIPLE (PARTICIPANT, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: PREVENTION
- Intervention
- DIETARY_SUPPLEMENT: Potassium Chloride|OTHER: Placebo
- Intervention Allocation
- Randomized
- Intervention Model
- Parallel
- Intervention Mask
- Triple
- Intervention Purpose
- Prevention
- Gender
- All
- Age
- Adult, Older_Adult
- Enrollment
- 25
- Outcome Measure
- Change in 24-hour systolic blood pressure (BP) from baseline to 12 weeks, Ambulatory blood pressure monitoring will be used to determine 24-hour systolic BP, 12 weeks
- Sponsor Collaborator
- Tulane University|National Institute of General Medical Sciences (NIGMS)
- Funded By
- OTHER
- Location
- Tulane University Office of Health Research, New Orleans, Louisiana, 70112, United States
- Other Id
- 2022-590|2P20GM109036-06A1
- Start Date
- 2023-03-29
- Primary Completion Date
- 2024-05-03
- Completion Date
- 2024-05-03
- First Posted
- 2023-03-07
- Results First Posted
- Last Update Posted
- 2024-05-07
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT05758142
- Title Cn
- Title En
- Potassium Intake-response Trial to Control Hypertension
- Bilingual Status
- semi_complete