Alcohol and energy drink
Dietary SupplementMultiple oral dose of alcohol Multiple oral dose of energy drink
NCT Number: NCT02771587
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.
Looking for future studies?
Notify Me18 year–45 year
All sexes
Interventional
Phase 1
IMIM, Barcelona, Spain
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Multiple oral dose of alcohol Multiple oral dose of energy drink
Multiple oral dose of alcohol
Multiple oral dose of energy drink
Multiple oral dose of water Multiple oral dose of non-caffeinated soft drink
Other names: Non-active treatment
Time frame: From baseline till 4 hours after administration
The total time outside the road will be measured in the tracking test
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
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
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
Time frame: From baseline till 8 hours after administration
Drunkenness will be measured using a visual analog scale (0-100 mm)
Time frame: From baseline till 8 hours after administration
Drowsiness will be measured using a visual analog scale (0-100 mm)
Time frame: From baseline till 8 hours after administration
Headache will be measured using a visual analog scale (0-100 mm)
Time frame: From baseline till 8 hours after administration
Palpitations will be measured using a visual analog scale (0-100 mm)
Time frame: From baseline till 8 hours after administration
Anxiety will be measured using a visual analog scale (0-100 mm)
Time frame: From baseline till 8 hours after administration
Subjective effects of alcohol and caffeine will be measured using Addiction Research Center Inventory
Time frame: From baseline till 8 hours after administration
Subjective effects of alcohol will be measured using BAES
Time frame: From baseline till 8 hours after administration
Systolic and diastolic blood pressure will be measured
Time frame: From baseline till 8 hours after administration
Heart rate will be measured
Time frame: From baseline till 8 hours after administration
Oral temperature will be measured
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
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
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
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
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
Time frame: From baseline till 8 hours after administration
Time frame: From baseline till 8 hours after administration
Time frame: From baseline till 8 hours after administration
Time frame: From baseline till 8 hours after administration
Time frame: From baseline till 8 hours after administration
Time frame: From baseline till 8 hours after administration
Time frame: From baseline till 2 hours after administration
Prothrombin time (PT) and ratio will be measured
Time frame: From baseline till 2 hours after administration
Activated partial thromboplastin time (APTT) and ratio will be measured
Time frame: From baseline till 2 hours after administration
Platelet function (PFA) will be measured
Time frame: From baseline till 2 hours after administration
Platelet count will be measured
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
Time frame: At the end of each experimental session
Drug liking will be measured using a visual analog scale (0-100 mm)
Parc de Salut Mar
Other
Effects of Alcohol and Energy Drinks on Driving Performance and Bleeding Risk
Acronym: AEDED
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.
Published trials that share one or more normalized conditions with this study.
NCT01847183
Alcohol-Related Disorders, Behavior
Eugene, Oregon, United States
View Trial DetailsNCT06629493
Alcohol Use Disorder (AUD), Alcohol-Related Disorders
Gijón, Principality of Asturias, Spain
View Trial DetailsNCT02911077
Alcohol-Related Disorders, Alcoholic Intoxication
Bethesda, Maryland, United States
View Trial DetailsNCT05121064
Acquired Immunodeficiency Syndrome, Alcohol-Related Disorders
Lusaka, Zambia
View Trial Details