Clinical TrialID 7898

Watermelon Dose Response Blood Pressure Study

NCT05892328

Pre-hypertension|Cardiovascular Diseases

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Record Fields

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Clinical Trial Id
7898
Evidence Id
7898
Core Evidence Id
7898
Source Clinical Trial Id
7896
Herb2 Clinical Trial Id
HBCT007896
Nct Id
NCT05892328
Title
Watermelon Dose Response Blood Pressure Study
Status
Active_Not_Recruiting
Phase
Study Result
No
Study Condition
Pre-hypertension|Cardiovascular Diseases
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: SINGLE (PARTICIPANT)|Primary Purpose: PREVENTION
Intervention
OTHER: Watermelon Flesh Dose 1|OTHER: Watermelon Flesh Dose 2|OTHER: Control
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Single
Intervention Purpose
Prevention
Gender
All
Age
Adult, Older_Adult
Enrollment
36
Outcome Measure
To evaluate the change in the dose response effects of watermelon flesh in regulating BP in individuals with pre-hypertension., This objective will be accomplished by assessing the 24-h Ambulatory Blood Pressure Machine (ABPM) in individuals with pre-hypertension before and after 4 weeks of watermelon flesh intake. Two doses of watermelon flesh will be tested (1 and 2 cup servings) compared to control., Baseline to 4 weeks
Sponsor Collaborator
Clinical Nutrition Research Center, Illinois Institute of Technology|National Watermelon Promotion Board
Funded By
INDUSTRY
Location
Clinical Nutrition Research Center, Chicago, Illinois, 60616, United States
Other Id
IRB-2023-03
Start Date
2023-04-07
Primary Completion Date
2023-12-01
Completion Date
2025-03-01
First Posted
2023-06-07
Results First Posted
Last Update Posted
2024-08-09
Study Document
Study Url
https://clinicaltrials.gov/study/NCT05892328
Title Cn
Title En
Watermelon Dose Response Blood Pressure Study
Bilingual Status
semi_complete