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Completed

NCT Number: NCT02771587

Interaction of Alcohol With Energy Drinks

The main objective of the project is to assess whether there is an interaction between the effects of ethanol and energy drinks on driving performance.

Secondary objectives include: to evaluate subjective effects (drunkenness) after administration of alcohol and energy drinks, to assess pharmacokinetics of alcohol, caffeine and taurine after alcohol and energy drinks administration and to assess if there is an increased risk of bleeding when both drinks are taken together.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

IMIM, Barcelona, Spain

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About this study

Consumption of energy drinks improve psychomotor performance and alertness. These drinks contain mostly caffeine, taurine and vitamins. Its consumption associated with ethanol may reduce feelings of drunkenness as the stimulant effects of caffeine could counteract the depressing effects of ethanol on the central nervous system. Reducing the perception of intoxication may predispose the intoxicated person to engage in risky behaviors such as driving under the influence of ethanol and therefore can increase the risk of a traffic accident. Furthermore, the combination of both beverages may increase the risk of bleeding in case of injury as anticoagulant effects have been described for ethanol while antiplatelet effects have been described for caffeine and taurine. A randomized clinical trial will be performed in healthy volunteers administering 4 treatment conditions: alcohol+energy drink, alcohol+placebo of energy drink, placebo of alcohol+energy drink and placebo of alcohol+placebo of energy drink. A multiple dose will be administered separated by 1 hour.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Understand and accept the study's procedures and sign an informed consent form
  • No evidence of somatic or psychiatric disorders as per past medical history and physical examination
  • EKG, blood and urine tests taken before entry into the study within the normal range. Minor and transient abnormalities may be acceptable if, according to the Principal Investigator's criterion and the state of the art, they are felt to have no clinical relevance, entail no danger to the participant, and don't interfere with the product's assessment. These abnormalities and their non-relevance must be specifically justified in writing)
  • Body mass index (BMI=weight/heigth2) between 19 and 27 kg/m2, weight between 50 and 100 kg
  • For premenopausal females, a regular menstrual cycle of 26-32 days duration.
  • Social or recreational alcohol consumption of at least 1 unit per day (or its equivalent [7 units] over the whole week) and having experienced drunkenness several times
  • Regular consumption of beverages containing methylxanthines (at least 5 per week)
  • Consumption of energy drinks several times previously
  • Having a driving license

Exclusion criteria

  • Evidence of a preexisting condition (including gastrointestinal, liver, or kidney disorders) that may alter the absorption, distribution, metabolism or excretion of the drug or symptoms suggestive of drug-induced gastrointestinal irritation
  • Previous psychiatric disorders, alcoholism, abuse of prescription drugs or illegal substances or regular consumption of psychoactive drugs
  • Having donated blood or having participated in this same study in the preceding 8 weeks, or having participated in any clinical trial with drugs in the preceding 12 weeks
  • Having had any somatic disease or having undergone major surgery in the 3 months prior to inclusion in the trial
  • Individuals intolerant or having experienced a severe adverse reaction to alcohol or energy drinks
  • Having regularly taken medication in the month before the trial, except for vitamins, herb-based remedies, dietary supplements that if, according to the Principal Investigator or his appointed collaborators' opinion, they pose no threat to the subjects and they won't interfere with the study's objectives. Single doses of symptomatic drugs taken during the week before the experimental session will not constitute an exclusion criterion if it can be assumed that it has been completely eliminated on the day of the experimental session
  • Smokers of >5 cigarettes/day
  • Consumption of >20 g/day of alcohol (females) or of >40 g/day (males)
  • Daily consumption of more than 5 coffees, teas, cola drinks or other stimulant or xanthine-containing beverages in the 3 months prior to inclusion in the study
  • Hepatitis B, hepatitis C or human immunodeficiency virus-positive individuals
  • Pregnant or lactating women, or those using hormonal or unreliable contraceptive methods during the study period. Complete abstinence, intrauterine devices, double barrier methods or a vasectomized sexual partner will be considered acceptable
  • Women with amenorrhea or suffering severe premenstrual syndrome
  • Individuals of Asian ascent

Treatment and study plan

Alcohol and energy drink

Dietary Supplement

Multiple oral dose of alcohol Multiple oral dose of energy drink

Alcohol

Dietary Supplement

Multiple oral dose of alcohol

Energy Drink

Dietary Supplement

Multiple oral dose of energy drink

Placebo

Dietary Supplement

Multiple oral dose of water Multiple oral dose of non-caffeinated soft drink

Other names: Non-active treatment

Primary outcomes

  1. Change in tracking test performance

    Time frame: From baseline till 4 hours after administration

    The total time outside the road will be measured in the tracking test

Secondary outcomes

  1. Change in simple reaction time (SRT)

    Time frame: From baseline till 4 hours after administration

    Test will be performed using the computerized cognitive testing battery CANTAB and mean latency will be measured

  2. Change in movement estimation

    Time frame: From baseline till 4 hours after administration

    The lapse of time between actual and predicted time will be measured in a movement estimation task

  3. Change in memory function

    Time frame: From baseline till 4 hours after administration

    The N-Back test will be performed with 2 different options: 0 back test and 2 back test

  4. Change in drunkenness

    Time frame: From baseline till 8 hours after administration

    Drunkenness will be measured using a visual analog scale (0-100 mm)

  5. Change in drowsiness

    Time frame: From baseline till 8 hours after administration

    Drowsiness will be measured using a visual analog scale (0-100 mm)

  6. Change in headache

    Time frame: From baseline till 8 hours after administration

    Headache will be measured using a visual analog scale (0-100 mm)

  7. Change in palpitations

    Time frame: From baseline till 8 hours after administration

    Palpitations will be measured using a visual analog scale (0-100 mm)

  8. Change in anxiety

    Time frame: From baseline till 8 hours after administration

    Anxiety will be measured using a visual analog scale (0-100 mm)

  9. Change in subjective effects measured with Addiction Research Center Inventory (ARCI)

    Time frame: From baseline till 8 hours after administration

    Subjective effects of alcohol and caffeine will be measured using Addiction Research Center Inventory

  10. Change in subjective effects measured with Biphasic alcohol effects scale (BAES)

    Time frame: From baseline till 8 hours after administration

    Subjective effects of alcohol will be measured using BAES

  11. Change in blood pressure

    Time frame: From baseline till 8 hours after administration

    Systolic and diastolic blood pressure will be measured

  12. Change in heart rate

    Time frame: From baseline till 8 hours after administration

    Heart rate will be measured

  13. Change in oral temperature

    Time frame: From baseline till 8 hours after administration

    Oral temperature will be measured

  14. Number of participants with serious and non-serious adverse events

    Time frame: From inclusion till one week after the last experimental session

    Collection of adverse effects spontaneously reported by the participants and/or observed by the investigators

  15. Area under the concentration-time curve (AUC 0-8h) of ethanol blood concentrations

    Time frame: From baseline till 8 hours after administration

    Calculation of AUC of ethanol concentrations obtained baseline and 0.25, 0.50h , 0.75, 1, 1.50, 1.75, 2, 2.25, 2.5, 3, 4, 6 and 8h after administration

  16. Area under the concentration-time curve (AUC 0-8h) of taurine blood concentrations

    Time frame: From baseline till 8 hours after administration

    Calculation of AUC of ethanol concentrations obtained baseline and 0.50,1, 1.50, 2, 4, 6 and 8h after administration

  17. Area under the concentration-time curve (AUC 0-8h) of caffeine blood concentrations

    Time frame: From baseline till 8 hours after administration

    Calculation of AUC of ethanol concentrations obtained baseline and 0,25, 0.50,1, 1.50, 2, 3, 4, 6 and 8h after administration

  18. Area under the concentration-time curve (AUC 0-8h) of ethanol breath air concentrations

    Time frame: From baseline till 8 hours after administration

    Calculation of AUC of ethanol concentrations obtained baseline and 0.25, 0.50, 0.75,1, 1.50, 1.75, 2, 2.25, 2.5, 3, 4, 6 and 8h after administration

  19. Maximum concentration (Cmax) of taurine

    Time frame: From baseline till 8 hours after administration

  20. Maximum concentration (Cmax) of ethanol

    Time frame: From baseline till 8 hours after administration

  21. Maximum concentration (Cmax) of caffeine

    Time frame: From baseline till 8 hours after administration

  22. Time to reach maximum concentration (tmax) of ethanol

    Time frame: From baseline till 8 hours after administration

  23. Time to reach maximum concentration (tmax) of caffeine

    Time frame: From baseline till 8 hours after administration

  24. Time to reach maximum concentration (tmax) of taurine

    Time frame: From baseline till 8 hours after administration

  25. Blood coagulation prothrombin

    Time frame: From baseline till 2 hours after administration

    Prothrombin time (PT) and ratio will be measured

  26. Blood coagulation thromboplastin

    Time frame: From baseline till 2 hours after administration

    Activated partial thromboplastin time (APTT) and ratio will be measured

  27. Platelet aggregation (function)

    Time frame: From baseline till 2 hours after administration

    Platelet function (PFA) will be measured

  28. Platelet count

    Time frame: From baseline till 2 hours after administration

    Platelet count will be measured

  29. Change in willingness to drive

    Time frame: From baseline till 6 hours after administration

    Willingness to drive in 3 different situations will be measured by means of a visual analog scale

  30. Like the drug (drink)

    Time frame: At the end of each experimental session

    Drug liking will be measured using a visual analog scale (0-100 mm)

Sponsors and collaborators

Lead sponsor

Parc de Salut Mar

Other

Registry information

Official study title

Effects of Alcohol and Energy Drinks on Driving Performance and Bleeding Risk

Acronym: AEDED

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
May 13, 2016
Registry last updated
Oct 19, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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