Clinical TrialID 943

Watermelon/UBIQuinone Study

NCT04972552

Kidney Transplantation

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Record Fields

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Clinical Trial Id
943
Evidence Id
943
Core Evidence Id
943
Source Clinical Trial Id
924
Herb2 Clinical Trial Id
HBCT000924
Nct Id
NCT04972552
Title
Watermelon/UBIQuinone Study
Status
Active_Not_Recruiting
Phase
Study Result
No
Study Condition
Kidney Transplantation
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: FACTORIAL|Masking: TRIPLE (PARTICIPANT, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: OTHER
Intervention
DIETARY_SUPPLEMENT: coenzyme Q10|OTHER: Watermelon diet|OTHER: Usual Diet|OTHER: Placebo
Intervention Allocation
Randomized
Intervention Model
Factorial
Intervention Mask
Triple
Intervention Purpose
Other
Gender
All
Age
Adult, Older_Adult
Enrollment
70
Outcome Measure
Number of patients who complete the study after randomized assignment, We will determine the number of patients who drop out of the study following randomized assignment, Measured at the 20 weeks mark|Number of participants who develop adverse safety events (including low systolic blood pressure or hyperkalemia) during participation in the study, We will measure the number of patients who develop low blood pressure and high potassium levels (hyperkalemia) following randomized assignment. Low blood pressure will be defined as systolic blood pressure \< 90 mmHg; hyperkalemia will be defined as serum potassium \> 5.5 meq/L, Measured from 0-20 weeks
Sponsor Collaborator
University of California, San Francisco
Funded By
OTHER
Location
University of California San Francisco, San Francisco, California, 94143, United States
Other Id
21-34366
Start Date
2021-11-15
Primary Completion Date
2024-12-30
Completion Date
2025-06-30
First Posted
2021-07-22
Results First Posted
Last Update Posted
2024-06-20
Study Document
Study Url
https://clinicaltrials.gov/study/NCT04972552
Title Cn
Title En
Watermelon/UBIQuinone Study
Bilingual Status
semi_complete