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The Effect of Energy Drink Ingredients on Cardiovascular Function in Men and Women 18-39 Years Old (EEDICF)

Primary Purpose

Cardiac Arrhythmia, Blood Pressure

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Energy Drink Ingredients and Exercise
Sponsored by
Duquesne University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Cardiac Arrhythmia focused on measuring caffeine, taurine, carnitine, energy drink

Eligibility Criteria

18 Years - 39 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. No preexisting medical conditions (including pregnancy)
  2. Subjects must be capable of exercising on a treadmill (Vigorous activity: more than 7 kcal/min; https://www.cdc.gov/nccdphp/dnpa/physical/pdf/PA_Intensity_table_2_1.pdf)
  3. BMI within normal range (18.5 - 24.9 kg/m2)
  4. Average daily caffeine intake between 1 and 5 caffeinated beverages

Exclusion Criteria:

  1. Age below 18 or greater than 39 years
  2. Unable to provide legal consent to participate in the study
  3. Preexisting medical conditions including but not limited to: pregnancy, cardiovascular disease, endocrine disorders, psychiatric or neurological disorders, musculo-skeletal disorders, immune disorders, respiratory disorders, dermatological disorders, infections, blindness, hearing disabilities
  4. BMI less than 18.5 or greater than 24.9 kg/m25.
  5. Current or future students of Drs. Johnson and/or Montepara
  6. Incarceration in local, state or federal justice systems

Sites / Locations

  • Duquesne UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Changes in BP, HR and EKG with Test Solution A and Exercise

Changes in BP, HR and EKG with Test Solution B and Exercise

Changes in BP, HR and EKG with Test Solution C and Exercise

Changes in BP, HR and EKG with Test Solution C

Arm Description

Subject baseline HR, BP, EKG recorded. Subject will ingest sucrose (150g): 30 min later, subject will exercise on a treadmill Subjects will return each week to repeat the above procedures with a different test solution.

Subject baseline HR, BP, ECG recorded. Subject will ingest sucrose (150g); caffeine (400 mg) 30 min later, subject will exercise on a treadmill Subjects will return each week to repeat the above procedures with a different test solution.

Subject baseline HR, BP, ECG recorded. Subject will ingest sucrose (150g); caffeine (400 mg); taurine (4,000 mg); carnitine (400 mg) 30 min later, subject will exercise on a treadmill

Subject baseline HR, BP, ECG recorded. Subject will ingest sucrose (150g); caffeine (400 mg); taurine (4,000 mg); carnitine (400 mg)

Outcomes

Primary Outcome Measures

Change in QTc interval of EKG
Lengthening or shortening of the corrected QT interval (QTc) of the subject EKG at 1, 2, and 4 hours post treatment will be compared to pre-treatment measurements. The QTc will be calculated utilizing Bezett's formula.

Secondary Outcome Measures

Change in Heart Rate
Increase or decrease in heart rate at 1, 2, and 4 hours post treatment compared to pre-treatment. Measurements of heart rate will be taken utilizing an automated sphygmomanometer
Change in Systolic and Diastolic Blood Pressure
Increase or decrease in systolic and diastolic blood pressure at 1, 2, and 4 hours post treatment compared to pre-treatment. Measurements of heart rate will be taken utilizing an automated sphygmomanometer.

Full Information

First Posted
October 31, 2019
Last Updated
March 19, 2021
Sponsor
Duquesne University
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1. Study Identification

Unique Protocol Identification Number
NCT04149717
Brief Title
The Effect of Energy Drink Ingredients on Cardiovascular Function in Men and Women 18-39 Years Old
Acronym
EEDICF
Official Title
The Effect of Energy Drink Ingredients on Cardiovascular Function
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2020 (Actual)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
March 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duquesne University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Statement of the research question: Does the caffeine in energy drinks interact with other ingredients to affect cardiovascular function in healthy male and female adults after exercise? Purpose and significance of the study: Energy drinks are beverages promoted to enhance alertness along with athletic and cognitive performance. The most common ingredients found in energy drinks include water, sugar, caffeine, taurine, and B-vitamins, with variable inclusion of other ingredients, such as carnitine, glucuronolactone, inositol, guarana, ginkgo biloba leaf extract, thistle extract, and ginseng root extract. Since the mid-1990s, the consumption of energy drinks has grown dramatically, with worldwide sales in 2017 exceeding $49 billion. As the sale of energy drinks has grown, so has the number of adverse event case reports for patients who consumed energy drinks. Reported symptoms included cardiac arrhythmias such as ventricular fibrillation, atrial fibrillation, and cardiac arrest. A few small clinical studies have found that energy drinks can increase systolic and diastolic blood pressure and change electrical activity in the heart as measured by an electrocardiogram (ECG). The intent of the proposed study is to determine whether caffeine or the combination of caffeine with taurine and L-carnitine can alter cardiovascular function. Hypothesis: The effects of the ingredients of energy drinks on the heart are mediated in part by interactions between caffeine, taurine and carnitine. The amount of each ingredient in the study was based upon the amount commonly contained in two cans of energy drinks currently on the market.
Detailed Description
Title: The Effect of Energy Drink Ingredients on Cardiovascular Function Statement of the research question Does the caffeine in energy drinks interact with other ingredients to affect cardiovascular function, including QTc interval of the EKG, heart rate and blood pressure in healthy male and female adults after exercise? Purpose and significance of the study Energy drinks are beverages promoted to enhance alertness along with athletic and cognitive performance. The most common ingredients found in energy drinks include water, sugar, caffeine, taurine, and B-vitamins, with variable inclusion of other ingredients, such as carnitine, glucuronolactone, inositol, guarana, ginkgo biloba leaf extract, thistle extract, and ginseng root extract. Since the mid-1990s, the consumption of energy drinks has grown dramatically, with worldwide sales in 2017 exceeding $49 billion. As the sale of energy drinks has grown, so has the number of adverse event case reports for patients who consumed energy drinks. Reported symptoms include cardiac arrhythmias such as ventricular fibrillation, atrial fibrillation, and cardiac arrest. A few small clinical studies have reported that energy drinks can increase systolic and diastolic blood pressure and change electrical activity in the heart as measured by an electrocardiogram (EKG). The intent of the proposed study is to determine whether caffeine or the combination of caffeine with taurine and L-carnitine can alter heart rate, blood pressure and the QTc interval of the EKG. Caffeine stimulates cardiovascular function primarily through antagonism of adenosine receptors. Taurine is a modulator of intracellular calcium ion concentrations which can affect the strength cardiac contraction. Carnitine facilitates fatty acid transport into the mitochondria, thereby increasing the production of adenosine triphosphate, the energy source of cells. Hypothesis: the effects of the ingredients of energy drinks on the heart are mediated in part by interactions between caffeine, taurine and carnitine. The amount of each ingredient in the study was based upon the amount commonly contained in two cans of energy drinks currently on the market.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Arrhythmia, Blood Pressure
Keywords
caffeine, taurine, carnitine, energy drink

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
repeated measures, crossover design
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
The three test solutions will be coded as "A", "B" and "C". Both the subject and the provider of the test solution to the subject will be blinded to the ingredients in the solution. The person who provides the test solution will be blind to the identity of the subject other than by subject number. The person who analyzes the data will be blinded to subject identity and which test solution was administered. The key for the test solutions and subject identity will be kept in a locked drawer in the office of the principal investigator.
Allocation
Randomized
Enrollment
35 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Changes in BP, HR and EKG with Test Solution A and Exercise
Arm Type
Experimental
Arm Description
Subject baseline HR, BP, EKG recorded. Subject will ingest sucrose (150g): 30 min later, subject will exercise on a treadmill Subjects will return each week to repeat the above procedures with a different test solution.
Arm Title
Changes in BP, HR and EKG with Test Solution B and Exercise
Arm Type
Experimental
Arm Description
Subject baseline HR, BP, ECG recorded. Subject will ingest sucrose (150g); caffeine (400 mg) 30 min later, subject will exercise on a treadmill Subjects will return each week to repeat the above procedures with a different test solution.
Arm Title
Changes in BP, HR and EKG with Test Solution C and Exercise
Arm Type
Experimental
Arm Description
Subject baseline HR, BP, ECG recorded. Subject will ingest sucrose (150g); caffeine (400 mg); taurine (4,000 mg); carnitine (400 mg) 30 min later, subject will exercise on a treadmill
Arm Title
Changes in BP, HR and EKG with Test Solution C
Arm Type
Experimental
Arm Description
Subject baseline HR, BP, ECG recorded. Subject will ingest sucrose (150g); caffeine (400 mg); taurine (4,000 mg); carnitine (400 mg)
Intervention Type
Dietary Supplement
Intervention Name(s)
Energy Drink Ingredients and Exercise
Intervention Description
Subject will ingest 500 mL of one of three test solutions: A) sucrose (150g) B) sucrose (150g); caffeine (400 mg) C) sucrose (150g); caffeine (400 mg); taurine (4,000 mg); carnitine (400 mg) 3. 30 min later, subject will exercise on a treadmill using the Bruce Protocol maximum exercise test (https://www.aopa.org/go-fly/medical-resources/health-conditions/heart-and-circulatory-system/bru...). For one additional session, subjects will receive test solution C without exercise. 4. Each stage will last 3 minutes. Stage 1 = 1.7 mph at 2% Grade Stage 2 = 2.5 mph at 4% Grade Stage 3 = 3.4 mph at 6% Grade Stage 4 = 4.2 mph at 8% Grade Stage 5 = 5.0 mph at 10% Grade Stage 6 = 5.5 mph at 12% Grade Stage 7 = 6.0 mph at 14% Grade Stage 8 = 6.5 mph at 15% Grade Stage 9 = 7.0 mph at 15% Grade. The test will end when subjects reach exhaustion. 5. 1, 2, and 4 hrs following ingestion, HR, BP, and EKG will be recorded.
Primary Outcome Measure Information:
Title
Change in QTc interval of EKG
Description
Lengthening or shortening of the corrected QT interval (QTc) of the subject EKG at 1, 2, and 4 hours post treatment will be compared to pre-treatment measurements. The QTc will be calculated utilizing Bezett's formula.
Time Frame
0, 1, 2, 4, hours post-dose
Secondary Outcome Measure Information:
Title
Change in Heart Rate
Description
Increase or decrease in heart rate at 1, 2, and 4 hours post treatment compared to pre-treatment. Measurements of heart rate will be taken utilizing an automated sphygmomanometer
Time Frame
0, 1, 2, 4, hours post-dose
Title
Change in Systolic and Diastolic Blood Pressure
Description
Increase or decrease in systolic and diastolic blood pressure at 1, 2, and 4 hours post treatment compared to pre-treatment. Measurements of heart rate will be taken utilizing an automated sphygmomanometer.
Time Frame
0, 1, 2, 4, hours post-dose

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
39 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: No preexisting medical conditions (including pregnancy) Subjects must be capable of exercising on a treadmill (Vigorous activity: more than 7 kcal/min; https://www.cdc.gov/nccdphp/dnpa/physical/pdf/PA_Intensity_table_2_1.pdf) BMI within normal range (18.5 - 24.9 kg/m2) Average daily caffeine intake between 1 and 5 caffeinated beverages Exclusion Criteria: Age below 18 or greater than 39 years Unable to provide legal consent to participate in the study Preexisting medical conditions including but not limited to: pregnancy, cardiovascular disease, endocrine disorders, psychiatric or neurological disorders, musculo-skeletal disorders, immune disorders, respiratory disorders, dermatological disorders, infections, blindness, hearing disabilities BMI less than 18.5 or greater than 24.9 kg/m25. Current or future students of Drs. Johnson and/or Montepara Incarceration in local, state or federal justice systems
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
David A Johnson, Ph.D.
Phone
412-396-5952
Email
johnsond@duq.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Courtney Montepara, Pharm.D.
Phone
412-396-4335
Email
monteparac@duq.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Delmonico, Ph.D.
Organizational Affiliation
Institutional Review Board, Chair, Duquesne University
Official's Role
Study Chair
Facility Information:
Facility Name
Duquesne University
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15282
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David A Johnson, Ph.D.
Phone
412-396-5952
Email
johnsond@duq.edu
First Name & Middle Initial & Last Name & Degree
Courtney Montepara, Pharm.D.
Phone
4123964335
Email
monteparac@duq.edu

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
28446495
Citation
Fletcher EA, Lacey CS, Aaron M, Kolasa M, Occiano A, Shah SA. Randomized Controlled Trial of High-Volume Energy Drink Versus Caffeine Consumption on ECG and Hemodynamic Parameters. J Am Heart Assoc. 2017 Apr 26;6(5):e004448. doi: 10.1161/JAHA.116.004448.
Results Reference
background
PubMed Identifier
27162113
Citation
Kozik TM, Shah S, Bhattacharyya M, Franklin TT, Connolly TF, Chien W, Charos GS, Pelter MM. Cardiovascular responses to energy drinks in a healthy population: The C-energy study. Am J Emerg Med. 2016 Jul;34(7):1205-9. doi: 10.1016/j.ajem.2016.02.068. Epub 2016 Mar 2.
Results Reference
background
PubMed Identifier
24176062
Citation
Goldfarb M, Tellier C, Thanassoulis G. Review of published cases of adverse cardiovascular events after ingestion of energy drinks. Am J Cardiol. 2014 Jan 1;113(1):168-72. doi: 10.1016/j.amjcard.2013.08.058. Epub 2013 Oct 4.
Results Reference
background
PubMed Identifier
31137991
Citation
Shah SA, Szeto AH, Farewell R, Shek A, Fan D, Quach KN, Bhattacharyya M, Elmiari J, Chan W, O'Dell K, Nguyen N, McGaughey TJ, Nasir JM, Kaul S. Impact of High Volume Energy Drink Consumption on Electrocardiographic and Blood Pressure Parameters: A Randomized Trial. J Am Heart Assoc. 2019 Jun 4;8(11):e011318. doi: 10.1161/JAHA.118.011318. Epub 2019 May 29.
Results Reference
background
PubMed Identifier
26828774
Citation
Longo N, Frigeni M, Pasquali M. Carnitine transport and fatty acid oxidation. Biochim Biophys Acta. 2016 Oct;1863(10):2422-35. doi: 10.1016/j.bbamcr.2016.01.023. Epub 2016 Jan 29.
Results Reference
background
PubMed Identifier
28756014
Citation
Turnbull D, Rodricks JV, Mariano GF, Chowdhury F. Caffeine and cardiovascular health. Regul Toxicol Pharmacol. 2017 Oct;89:165-185. doi: 10.1016/j.yrtph.2017.07.025. Epub 2017 Jul 26.
Results Reference
background
PubMed Identifier
9635023
Citation
Satoh H. Cardiac actions of taurine as a modulator of the ion channels. Adv Exp Med Biol. 1998;442:121-8. doi: 10.1007/978-1-4899-0117-0_16.
Results Reference
background
Links:
URL
https://www.statista.com/statistics/621710/energy-drink-consumption-frequency-in-the-us-by-age/
Description
Energy drink consumption frequency in the U.S. 2016, by age
URL
http://www.nutritionaloutlook.com/hero/614473
Description
Energy Drink Sales
URL
https://www.aopa.org/go-fly/medical-resources/health-conditions/heart-and-circulatory-system/bruce-protocol-stress-test
Description
Bruce Protocol Stress Test
URL
https://www.cdc.gov/nccdphp/dnpa/physical/pdf/PA_Intensity_table_2_1.pdf
Description
General Physical Activities Defined by Level of Intensity

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The Effect of Energy Drink Ingredients on Cardiovascular Function in Men and Women 18-39 Years Old

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