Evaluation of Energy Drinks on Electrocardiographic, Vascular and Hematologic Parameters in Healthy Volunteers

Evaluation of Energy Drink Consumption on Electrocardiographic, Vascular and Hematologic Parameters in Young Healthy Volunteers: A Randomized, Double Blind, Active-Controlled, Crossover Study

This study will determine the cardiovascular effects of energy drink consumption in healthy individuals through electrocardiogram (ECG), central blood pressure assessment, and ROTEM® analysis.

Study Overview

Detailed Description

This is a randomized, double blind, controlled, crossover study evaluating the electrocardiographic, blood pressure, and hematological effects of an energy drink.

  • Subjects who have contacted the PI/AI/SC for consideration of participation in this study will be scheduled a time to come to the Clinical Investigation Facility (CIF) Interview Room, which is a private room located on the David Grant Medical Center campus, for an initial evaluation for inclusion eligibility determination.
  • At the initial evaluation subjects will be informed about the details of the study, be presented with the Informed Consent Document (ICD) and HIPAA documents and be asked to sign the appropriate forms voluntarily if they want to be a part of this study. Once consented, subjects will then be asked a series of questions to see if they qualify for inclusion in the study. A baseline ECG, Chem 7, and a peripheral blood pressure will be obtained to rule out everything but normal sinus rhythm, normal potassium level, and blood pressure less than 140/90. A cardiologist will approve every baseline ECG to allow the participant to enroll in the study.
  • If the subject meets inclusion criteria and are approved by the cardiologist, they will be enrolled, and allocated a randomized participant ID number. They will also be given the "Participant Instruction Sheet".
  • Participants will be asked to document their normal baseline caffeine consumption on the initial questionnaire.
  • Participants will randomly be assigned to consume either two-16 oz. containers of Monster Energy® drink, original flavor, two-16 oz. containers of an active control drink, or two 16 oz. containers of a placebo drink during their first day of treatment.
  • The blinding and randomization will be performed by a member of the pharmacy staff who will have the randomization code in a sealed envelope in the pharmacy. The PI, AIs and SC will be blinded. In the event of a medical emergency, unblinding a particular subject may occur upon request to the pharmacy staff from an investigator or study coordinator. Only the requested subject will be unblinded.
  • The control drinks will comprise an equivalent volume. The active control drink 16 oz. bottle will contain: 200 mg moxifloxacin (dissolved tablet), carbonated water, reconstituted lime juice (readily available from supermarkets), and cherry flavoring (regularly used flavoring in compounding). The placebo drink will be the same except it will not contain moxifloxacin.
  • The energy drink and control drinks will be repackaged by a member of the pharmacy staff in identical 16 oz. bottles and checked by another staff member. The active and control drinks will be made at least 24 hours but no more than 7 days in advance and will be stored in a refrigerator in a designated area within the inpatient pharmacy. Study drinks will be available for the investigator/coordinator for distribution to the participants.
  • Participants will be informed on the "Participant Instruction Sheet" to refrain from caffeine or energy drink consumption for 48 hours prior to study days 1, 8, and 15. They will need to have similar work shifts 48 hours before each study day (i.e. day or night shift). In addition, participants will be instructed to be in the fasting state (no food or drink other than water) for 12 hours prior to study days 1, 8, and 15.
  • On day 1, a baseline ECG, HR, peripheral and central blood pressures, and lab draw will be obtained prior to consumption of the assigned study drink. The lab draw will be used to determine baseline clotting time using ROTEM® analysis. After completion of baseline readings, subjects will have 45 minutes to consume two-16 oz. containers of Monster Energy® or either control drink as assigned. The time clock for study duration will start when the participant is issued their study drink. Repeat measurements of ECG, HR, peripheral and central blood pressures will be performed at 1, 2, 4, and 6 hours. In addition, a second lab draw will be taken at 2 hours and submitted for ROTEM® analysis to determine clotting time. At 2 hours the subject will also be provided a study-controlled breakfast. During each measurement session, participants will also be asked to "describe any adverse effects you may be experiencing". All measurements taken and responses from participants will be annotated on the participant treatment form.
  • Participants may eat after lunch between hours four and five after the energy drink was consumed. They will be asked to eat approximately the same meals for lunch on the 3 study days. They may not consume additional caffeine or energy drinks not provided by the study group until after the measurements are taken 6 hours later.
  • A minimum 6-day wash-out period must elapse prior to initiation of the second phase of the study, at which time the same treatment/monitoring process will occur (i.e. Day 8 or after). It will again be repeated on day 15 or after.
  • Measurements will include: ECG, BP, lab draw, and questions about side effects each participant may be experiencing.

Study Type

Interventional

Enrollment (Actual)

2

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • Travis Air Force Base, California, United States, 94535
        • David Grant Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Healthy male and female, active duty military service members or DoD beneficiaries, who are eligible to receive care at DGMC.
  • Ages 18-40 years old.
  • Participants must be willing to refrain from caffeine and energy drink use 48 hours prior to study days 1, 8, and 15

Exclusion Criteria:

  • In an effort to recruit subjects in general good health, those with the following medical conditions or disease states will be excluded from enrollment:

    • Cardiovascular risk factors: Heart rhythm other than normal sinus, history of atrial or ventricular arrhythmia, family history of premature sudden cardiac death before the age of 60, left ventricular hypertrophy, acute myocardial ischemia, atherosclerosis, hypertension, palpitations, T-wave abnormalities, baseline corrected QT (QTc) interval greater than 440 milliseconds(ms). This will be determined on the ECG obtained during initial screening appointment, and reviewed by cardiologist and through the questionnaire responses of the participant.
    • Blood pressure at initial screening appointment or at baseline on study Day 1 greater than 140/90
    • Hypokalemia or liver abnormalities (AST/ALT abnormality) identified at initial appointment when baseline lab values will be drawn.
    • Presence of any known medical condition, confirmed through participant interview up to the discretion of the research team. Examples of these are:
  • Hypertension
  • Thyroid disease
  • Type 1 or 2 diabetes mellitus
  • Recurrent headaches
  • Depression, currently receiving treatment (due to possible drug interactions)
  • Any psychiatric condition or neurological disorder including seizures
  • History of alcohol or drug abuse in the previous 5 years
  • Ever been diagnosed or told they have or had renal or hepatic dysfunction

    • Concurrent use of ANY medication taken in an amount greater than twice a week, to include herbal products or supplements, NOT TO INCLUDE hormonal contraceptives. If less than or equal to 2 days per week, the investigator will determine if the subject is to be included or excluded based on the available literature for that medication.
    • Pregnant or lactating females will be excluded from participation with urine dipstick tests used to confirm pregnancy (pregnancy test performed before each treatment session, days 1, 8 and 15)
    • All non-English speaking / writing subjects and those that do not understand the study or consent process will be excluded from the study due to unavailability of medical qualified translator at all times during the study.
    • If the subject refuses to sign the informed consent document or HIPAA Authorization, they will be excluded as well.
    • Allergy to any substance in the study design.
    • Any other medical reason that at the discretion of the investigators would pose a risk to the health of the subject.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Energy drink
Two 16 oz bottles of energy drink will be consumed at baseline.
32oz of commercially available energy drink
Active Comparator: Moxifloxacin control
32oz of active control drink will contain 400mg moxifloxacin with inactive flavoring ingredients.
400mg moxifloxacin active control drink
Other Names:
  • active control
Placebo Comparator: placebo control
32oz placebo control drink
Placebo drink

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
QTc interval change from baseline in each of 3 arms
Time Frame: 1 hour post consumption
1 hour post consumption
Central systolic blood pressure change from baseline in each of 3 arms
Time Frame: 1 hour post consumption
1 hour post consumption
Peripheral systolic blood pressure change from baseline in each of 3 arms
Time Frame: 1 hour post consumption
1 hour post consumption
QTc interval change from baseline in each of 3 arms
Time Frame: 2 hours post consumption
2 hours post consumption
QTc interval change from baseline in each of 3 arms
Time Frame: 4 hours post consumption
4 hours post consumption
QTc interval change from baseline in each of 3 arms
Time Frame: 6 hours post consumption
6 hours post consumption
central systolic blood pressure change from baseline in each of 3 arms
Time Frame: 2 hours post consumption
2 hours post consumption
central systolic blood pressure change from baseline in each of 3 arms
Time Frame: 4 hours post consumption
4 hours post consumption
central systolic blood pressure change from baseline in each of 3 arms
Time Frame: 6 hours post consumption
6 hours post consumption
Peripheral systolic blood pressure change from baseline in each of 3 arms
Time Frame: 2 hours post consumption
2 hours post consumption
Peripheral systolic blood pressure change from baseline in each of 3 arms
Time Frame: 4 hours post consumption
4 hours post consumption
Peripheral systolic blood pressure change from baseline in each of 3 arms
Time Frame: 6 hours post consumption
6 hours post consumption

Secondary Outcome Measures

Outcome Measure
Time Frame
Thromboelastometry changes from baseline in each of 3 arms
Time Frame: 2 hours post consumption
2 hours post consumption
ECG parameter changes from baseline in each of 3 arms
Time Frame: 1 hour post consumption
1 hour post consumption
ECG parameter changes from baseline in each of 3 arms
Time Frame: 2 hours post consumption
2 hours post consumption
ECG parameter changes from baseline in each of 3 arms
Time Frame: 4 hours post consumption
4 hours post consumption
ECG parameter changes from baseline in each of 3 arms
Time Frame: 6 hours post consumption
6 hours post consumption

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sarah Kelly, PharmD, David Grant Medical Center

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 26, 2017

Primary Completion (Actual)

March 13, 2018

Study Completion (Actual)

March 13, 2018

Study Registration Dates

First Submitted

January 11, 2017

First Submitted That Met QC Criteria

January 12, 2017

First Posted (Estimate)

January 16, 2017

Study Record Updates

Last Update Posted (Actual)

April 7, 2020

Last Update Submitted That Met QC Criteria

April 3, 2020

Last Verified

April 1, 2020

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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