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NCT05892328 · ClinicalTrials.gov registry record · NA
Watermelon Dose Response Blood Pressure Study
A NA study of Cardiovascular Diseases and Pre Hypertension, sponsored by Clinical Nutrition Research Center, Illinois Institute of Technology.
- Active
- Registry status
- NA
- Development phase
- 36
- Enrollment target
- 1
- Study location
NCT05892328 is a NA study of Cardiovascular Diseases and Pre Hypertension that is active but no longer recruiting, run by Clinical Nutrition Research Center, Illinois Institute of Technology. The registered enrollment target is 36 participants, below the 26,974-participant average among 300 other Cardiovascular Diseases trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05892328, a NA study of Cardiovascular Diseases and Pre Hypertension, is active but no longer recruiting, sponsored by Clinical Nutrition Research Center, Illinois Institute of Technology.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
- 1
- Study location
Study Summary
1. Primary outcome: To evaluate the dose response effects of watermelon flesh in regulating Blood Pressure (BP) in individuals with pre-hypertension. 2. Secondary outcomes: To study the dose-response effects of watermelon flesh intake on cardio-metabolic risk factors including plasma metabolic markers, lipid profile and nitrate/nitrite levels in individuals with pre-hypertension.
Conditions Studied
Interventions
- OTHER Control
- OTHER Watermelon Flesh Dose 1
- OTHER Watermelon Flesh Dose 2
Study Locations (1)
Illinois
- Clinical Nutrition Research Center - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2023-04-07 |
| Est. Completion | 2026-03-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05892328
The ClinicalTrials.gov registry entry for NCT05892328 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 26,974-participant average among 300 other Cardiovascular Diseases trials with a reported enrollment target (100% lower). The listed sponsor is Clinical Nutrition Research Center, Illinois Institute of Technology, which has 59 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Cardiovascular Diseases appearing as the primary indexed condition, and to 3 interventions - of which Control is the first listed.
NCT05892328 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.
Frequently Asked Questions
What is clinical trial NCT05892328 about?
NCT05892328 is a clinical study titled "Watermelon Dose Response Blood Pressure Study". 1. Primary outcome: To evaluate the dose response effects of watermelon flesh in regulating Blood Pressure (BP) in individuals with pre-hypertension. 2. Secondary outcomes: To study the dose-response effects of watermelon flesh intake on cardio-metabolic risk factors including plasma metabolic marke...
What is the current status of trial NCT05892328?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 36 participants. The study started on 2023-04-07. Estimated completion is 2026-03-01.
What conditions does trial NCT05892328 study?
This clinical trial studies the following conditions: Cardiovascular Diseases, Pre Hypertension.
What interventions are being tested in trial NCT05892328?
The interventions under investigation include: Control (OTHER), Watermelon Flesh Dose 1 (OTHER), Watermelon Flesh Dose 2 (OTHER).
Who is sponsoring clinical trial NCT05892328?
This trial is sponsored by Clinical Nutrition Research Center, Illinois Institute of Technology, which has 59 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05892328 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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