The Effect of Energy Drink on Cardiovascular Variables: A Randomized Controlled Trial
Completed · Not applicable · Has a placebo group
Conditions studied: Cardiovascular Diseases
In brief
Many adults in the United States regularly consumer energy drinks. Currently, the safety of energy drinks is still questionable and there are many reports associating energy drinks with adverse events including hospitalizations and deaths. Previous research shows that energy drink can affect heart rhythm and elevate blood pressure. However, these studies use a higher volume (32 ounces) of energy drinks than those available in the market (24 ounces). The purpose of this study is to study if 24-ounce energy drinks can significantly affect heart rhythm and elevate blood pressure when compared to a placebo.
Key facts
- Study ID
- NCT03841838
- Run by
- University of the Pacific
- People needed
- 20
- Starts
- 2019-02-23
- Expected to finish
- 2019-05-09
- Last updated by the study team
- 2019-09-25
Who can join
Age: 18 and older, up to 40. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy male or female adults 18-40 years old
- Participants must be willing to refrain from caffeine and alcohol use 48 hours prior to each study day
- Participants must be willing to fast 10 hours prior to each study day
- Participants must have health insurance
You may not qualify if…
- Corrected QT (QTc) interval greater than 450 milliseconds (ms). QTc will be determined on the ECG obtained during initial screening appointment.
- Blood pressure at initial screening appointment greater than 140/90 mmHg.
- Presence of any known medical condition confirmed through participant interview
- Concurrent use of ANY medication taken on a daily basis, to include herbal products or supplements (exception include oral contraceptives that will be allowed if taking for longer than 1 month)
- Current smokers or those who have smoked any cigarettes within the past month
- Pregnant or currently breastfeeding
Where it is running
- University of Pacific — Stockton, California, United States
Full record on ClinicalTrials.gov
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