Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Recruitment Status
NOT_YET_RECRUITING
Clinical Phase
PHASE2
Total Enrollment
35 participants
Study Classification
INTERVENTIONAL
Study Start Date
2024-12-01
Study Completion Date
2025-02-07
Brief Summary
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Study Title: Nutritional Supplement to Rapidly Decrease Blood Alcohol Concentration (BAC): Safety and Efficacy Study Design: Double-blind, randomized, placebo-controlled clinical trial Objective: Evaluate safety and efficacy of a nutritional supplement to rapidly decrease blood alcohol concentration (BAC), alcohol-induced impairment, and hangover symptoms after excessive alcohol consumption.
Primary Outcomes:
BAC reduction rate/extent (BACtrack S80™ breathalyzer) Cognitive/physical impairment change (DRUID app™)
Secondary Outcome:
Hangover symptom reduction (Acute Hangover Scale) Participants: 35 participants, recruited via social media Duration: 2 weeks, 2 testing sessions (4 hours each) Location: Closed facility in St. Petersburg, FL
Procedure:
Subjects consume standardized alcohol (1g ethanol/kg body weight) 40-minute drinking period BAC and impairment measurements Administration of test formulation or placebo
Measurements:
BAC: Baseline, 40min, 15min, 30min, 60min, 90min post-drinking Impairment: Baseline, 15min, 30min, 60min post-drinking Hangover: Next morning via text message
Safety Measures:
GRAS ingredients Lab testing of formulations Medical screening Adverse effect questionnaires Pregnancy tests BAC \<0.08% before leaving
Key Features:
Paired measurements: active vs. placebo for mini-drink and capsule formulations Uber transportation provided Strict inclusion/exclusion criteria
Data Analysis:
Electronic data entry Blinded submission for statistical analysis Paired comparisons and multiple statistical tests
This study aims to provide robust data on the efficacy in mitigating alcohol's effects, potentially offering a new tool for reducing alcohol-related impairment and hangover symptoms. The design prioritizes safety, consistency, and scientific rigor to ensure reliable results.
Primary Outcomes:
BAC reduction rate/extent (BACtrack S80™ breathalyzer) Cognitive/physical impairment change (DRUID app™)
Secondary Outcome:
Hangover symptom reduction (Acute Hangover Scale) Participants: 35 participants, recruited via social media Duration: 2 weeks, 2 testing sessions (4 hours each) Location: Closed facility in St. Petersburg, FL
Procedure:
Subjects consume standardized alcohol (1g ethanol/kg body weight) 40-minute drinking period BAC and impairment measurements Administration of test formulation or placebo
Measurements:
BAC: Baseline, 40min, 15min, 30min, 60min, 90min post-drinking Impairment: Baseline, 15min, 30min, 60min post-drinking Hangover: Next morning via text message
Safety Measures:
GRAS ingredients Lab testing of formulations Medical screening Adverse effect questionnaires Pregnancy tests BAC \<0.08% before leaving
Key Features:
Paired measurements: active vs. placebo for mini-drink and capsule formulations Uber transportation provided Strict inclusion/exclusion criteria
Data Analysis:
Electronic data entry Blinded submission for statistical analysis Paired comparisons and multiple statistical tests
This study aims to provide robust data on the efficacy in mitigating alcohol's effects, potentially offering a new tool for reducing alcohol-related impairment and hangover symptoms. The design prioritizes safety, consistency, and scientific rigor to ensure reliable results.
Detailed Description
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Study Title: Nutraceutical Safety and Efficacy Study
Introduction:
The nutraceutical Safety and Efficacy Study is a comprehensive clinical trial designed to evaluate a novel formulation aimed at rapidly decreasing blood alcohol concentration (BAC), alcohol-induced impairment, and veisalgia (hangover) symptoms following excessive alcohol consumption. This study addresses a significant public health concern by potentially offering a method to mitigate the negative effects of alcohol overconsumption.
Study Design:
This is a triple-blinded, randomized, placebo-controlled clinical trial. The triple-blind nature ensures that the subjects, investigators, and data analysts are unaware of the treatment assignments, minimizing bias in the results.
Primary Objectives:
To determine the rate and extent of BAC reduction after administration of nutraceutical compared to placebo.
To assess the change in cognitive and physical impairment due to nutraceutical supplement after excessive alcohol consumption.
Secondary Objective:
To evaluate the reduction in hangover symptoms the morning after excessive alcohol consumption when active compared to placebo.
Study Population:
The study will recruit 70 subjects (35 per arm) from the Tampa Bay area through social media. Key inclusion criteria include:
Age 21 or older Regular social alcohol use Not naive to consuming more than 4 drinks at once Ability to attend all three sessions Ownership of a smartphone with texting capabilities
Exclusion criteria encompass:
Alcohol Use Disorder (AUDIT score ≥8) Use of certain medications (e.g., Antabuse, beta-lactam antibiotics) Current use of psychoactive products or illegal substances Active medical conditions precluding excessive alcohol use Pregnancy or unknown pregnancy status Current involvement in the criminal justice system
Study Duration and Timeline:
The study will span 4 weeks, with three testing sessions scheduled on Sundays: August 15th, August 22nd, and October 5th, 2024. Each session will last approximately 4 hours, from 4 PM to 8 PM. The final statistical analysis and preparation for journal submission are expected to be completed by early November 2024.
Study Location:
All sessions will be conducted at a centrally located closed bar in St. Petersburg, FL, ensuring a controlled environment for the study.
Intervention:
The study will test two formulations:
Capsule form Mini-drink form
Each formulation will be compared against a matching placebo. The active ingredients and placebos will be provided. The exact composition is proprietary, but it consists of Generally Recognized as Safe (GRAS) ingredients.
Study Procedure:
Each subject will participate in three sessions, receiving either the active formulation or placebo in a randomized order. The procedure for each session is as follows:
Subjects arrive and consume a standardized meal (one slice of pizza or equivalent).
Baseline measurements are taken (BAC and impairment tests). Subjects consume a 20 oz container of vodka and flavoring (1g ethanol per kg of body weight) over a 40-minute period.
Immediately after drinking, BAC is measured, and impairment tests are conducted.
Subjects receive either the active formulation or placebo. BAC measurements are taken at 15, 30, 60, and 90 minutes post-drinking. Impairment tests are conducted at 15, 30, and 60 minutes post-drinking. Subjects remain at the facility until their BAC is below 0.08%, then are provided Uber transportation home.
The following morning at 8 AM, subjects complete a hangover questionnaire via text message.
Outcome Measures:
Blood Alcohol Concentration (BAC):
Instrument: BACtrack S80™ breathalyzer (US FDA 510(k) approved) Measurement points: Baseline, immediately after drinking (40 minutes), then at 15, 30, 60, and 90 minutes post-drinking Analysis: Rate and extent of BAC reduction compared to placebo
Cognitive and Physical Impairment:
Primary instrument: DRUID app™
Secondary measures:
1. Horizontal Gaze Nystagmus (HGN) test
2. One-leg Stand test
3. Computer-assisted testing for reaction time, sustained attention, and decision making (www.HumanBenchMark.com) Measurement points: Baseline, 15, 30, and 60 minutes post-drinking Analysis: Change in impairment scores compared to placebo
Hangover Symptoms:
Instrument: Acute Hangover Scale (AHS™) Description: 9-question survey, rating symptoms on a scale of 0-7 Administration: Via text message at 8 AM the morning after each session Analysis: Comparison of hangover symptom scores between and placebo conditions
Safety Measures:
Use of GRAS ingredients in formulations Independent lab testing and certificate of analysis for all test formulations Thorough medical screening of subjects Administration of standardized adverse effect questionnaires Urine pregnancy tests for women of childbearing age before each session Ensuring subjects\' BAC is below 0.08% before leaving the facility Provision of Uber transportation to and from each session
Subject Consistency and Compliance:
To ensure physiological similarity across sessions, subjects will:
Drink a quart of water starting 4 hours before each session Refrain from eating or drinking (except water) for 4 hours before each session Consume the same standardized meal at the beginning of each session Agree to abstain from alcohol and euphoric substances for 24 hours after each session
Staffing:
A minimum of 14 support staff will be on-site to ensure efficient flow of subjects through each session. Dr. Gregory L. Smith and a medical assistant will conduct the physical impairment testing throughout the study sessions.
Data Collection and Management:
Data will be collected via a pre-prepared electronic data entry system for each individual subject. All data will be blinded and submitted electronically for separate statistical analysis.
Statistical Analysis:
The study will employ separate statistical analyses for paired comparisons of the capsule formulation and the mini-drink formulation. Multiple statistical tests will be conducted to determine statistical significance within the paired data, separately for each formulation and as combined data. The study aims for 80% statistical power with a p-value 0.05.
Ethical Considerations:
Institutional Review Board (IRB) approval will be obtained from the Medical Life Care Planners IRB.
The study will be registered on ClinicalTrials.gov and assigned a National Clinical Trial (NCT) number.
Informed consent will be obtained from all participants prior to study enrollment.
Subjects' privacy and data confidentiality will be maintained throughout the study.
Potential Impact:
If proven effective, could have significant implications for public health and safety. It could potentially:
Reduce the risk of alcohol-related accidents and injuries Mitigate productivity losses due to hangovers Provide a tool for responsible alcohol consumption
However, it's crucial to note that the product should not be seen as a means to enable excessive drinking or as a substitute for responsible alcohol consumption.
Limitations:
Single-center study, which may limit generalizability Relatively short duration of follow-up (next morning only) Potential for recall bias in self-reported hangover symptoms Unable to control for all factors that might influence alcohol metabolism or hangover severity (e.g., genetics, overall health status)
Future Directions:
Depending on the results of this initial study, future research could explore:
Long-term safety and efficacy Effects on different populations (e.g., varying age groups, ethnicities) Potential interactions with medications or medical conditions Optimal dosing and timing of administration Physiological mechanisms of action
Conclusion:
The Nutraceutical Safety and Efficacy Study represents a rigorous approach to evaluating a novel intervention for mitigating the effects of alcohol overconsumption. By employing a triple-blind, randomized, placebo-controlled design with multiple outcome measures, this study aims to provide robust evidence regarding the safety and efficacy. The results could have significant implications for public health strategies related to alcohol consumption and its associated risks.
Introduction:
The nutraceutical Safety and Efficacy Study is a comprehensive clinical trial designed to evaluate a novel formulation aimed at rapidly decreasing blood alcohol concentration (BAC), alcohol-induced impairment, and veisalgia (hangover) symptoms following excessive alcohol consumption. This study addresses a significant public health concern by potentially offering a method to mitigate the negative effects of alcohol overconsumption.
Study Design:
This is a triple-blinded, randomized, placebo-controlled clinical trial. The triple-blind nature ensures that the subjects, investigators, and data analysts are unaware of the treatment assignments, minimizing bias in the results.
Primary Objectives:
To determine the rate and extent of BAC reduction after administration of nutraceutical compared to placebo.
To assess the change in cognitive and physical impairment due to nutraceutical supplement after excessive alcohol consumption.
Secondary Objective:
To evaluate the reduction in hangover symptoms the morning after excessive alcohol consumption when active compared to placebo.
Study Population:
The study will recruit 70 subjects (35 per arm) from the Tampa Bay area through social media. Key inclusion criteria include:
Age 21 or older Regular social alcohol use Not naive to consuming more than 4 drinks at once Ability to attend all three sessions Ownership of a smartphone with texting capabilities
Exclusion criteria encompass:
Alcohol Use Disorder (AUDIT score ≥8) Use of certain medications (e.g., Antabuse, beta-lactam antibiotics) Current use of psychoactive products or illegal substances Active medical conditions precluding excessive alcohol use Pregnancy or unknown pregnancy status Current involvement in the criminal justice system
Study Duration and Timeline:
The study will span 4 weeks, with three testing sessions scheduled on Sundays: August 15th, August 22nd, and October 5th, 2024. Each session will last approximately 4 hours, from 4 PM to 8 PM. The final statistical analysis and preparation for journal submission are expected to be completed by early November 2024.
Study Location:
All sessions will be conducted at a centrally located closed bar in St. Petersburg, FL, ensuring a controlled environment for the study.
Intervention:
The study will test two formulations:
Capsule form Mini-drink form
Each formulation will be compared against a matching placebo. The active ingredients and placebos will be provided. The exact composition is proprietary, but it consists of Generally Recognized as Safe (GRAS) ingredients.
Study Procedure:
Each subject will participate in three sessions, receiving either the active formulation or placebo in a randomized order. The procedure for each session is as follows:
Subjects arrive and consume a standardized meal (one slice of pizza or equivalent).
Baseline measurements are taken (BAC and impairment tests). Subjects consume a 20 oz container of vodka and flavoring (1g ethanol per kg of body weight) over a 40-minute period.
Immediately after drinking, BAC is measured, and impairment tests are conducted.
Subjects receive either the active formulation or placebo. BAC measurements are taken at 15, 30, 60, and 90 minutes post-drinking. Impairment tests are conducted at 15, 30, and 60 minutes post-drinking. Subjects remain at the facility until their BAC is below 0.08%, then are provided Uber transportation home.
The following morning at 8 AM, subjects complete a hangover questionnaire via text message.
Outcome Measures:
Blood Alcohol Concentration (BAC):
Instrument: BACtrack S80™ breathalyzer (US FDA 510(k) approved) Measurement points: Baseline, immediately after drinking (40 minutes), then at 15, 30, 60, and 90 minutes post-drinking Analysis: Rate and extent of BAC reduction compared to placebo
Cognitive and Physical Impairment:
Primary instrument: DRUID app™
Secondary measures:
1. Horizontal Gaze Nystagmus (HGN) test
2. One-leg Stand test
3. Computer-assisted testing for reaction time, sustained attention, and decision making (www.HumanBenchMark.com) Measurement points: Baseline, 15, 30, and 60 minutes post-drinking Analysis: Change in impairment scores compared to placebo
Hangover Symptoms:
Instrument: Acute Hangover Scale (AHS™) Description: 9-question survey, rating symptoms on a scale of 0-7 Administration: Via text message at 8 AM the morning after each session Analysis: Comparison of hangover symptom scores between and placebo conditions
Safety Measures:
Use of GRAS ingredients in formulations Independent lab testing and certificate of analysis for all test formulations Thorough medical screening of subjects Administration of standardized adverse effect questionnaires Urine pregnancy tests for women of childbearing age before each session Ensuring subjects\' BAC is below 0.08% before leaving the facility Provision of Uber transportation to and from each session
Subject Consistency and Compliance:
To ensure physiological similarity across sessions, subjects will:
Drink a quart of water starting 4 hours before each session Refrain from eating or drinking (except water) for 4 hours before each session Consume the same standardized meal at the beginning of each session Agree to abstain from alcohol and euphoric substances for 24 hours after each session
Staffing:
A minimum of 14 support staff will be on-site to ensure efficient flow of subjects through each session. Dr. Gregory L. Smith and a medical assistant will conduct the physical impairment testing throughout the study sessions.
Data Collection and Management:
Data will be collected via a pre-prepared electronic data entry system for each individual subject. All data will be blinded and submitted electronically for separate statistical analysis.
Statistical Analysis:
The study will employ separate statistical analyses for paired comparisons of the capsule formulation and the mini-drink formulation. Multiple statistical tests will be conducted to determine statistical significance within the paired data, separately for each formulation and as combined data. The study aims for 80% statistical power with a p-value 0.05.
Ethical Considerations:
Institutional Review Board (IRB) approval will be obtained from the Medical Life Care Planners IRB.
The study will be registered on ClinicalTrials.gov and assigned a National Clinical Trial (NCT) number.
Informed consent will be obtained from all participants prior to study enrollment.
Subjects' privacy and data confidentiality will be maintained throughout the study.
Potential Impact:
If proven effective, could have significant implications for public health and safety. It could potentially:
Reduce the risk of alcohol-related accidents and injuries Mitigate productivity losses due to hangovers Provide a tool for responsible alcohol consumption
However, it's crucial to note that the product should not be seen as a means to enable excessive drinking or as a substitute for responsible alcohol consumption.
Limitations:
Single-center study, which may limit generalizability Relatively short duration of follow-up (next morning only) Potential for recall bias in self-reported hangover symptoms Unable to control for all factors that might influence alcohol metabolism or hangover severity (e.g., genetics, overall health status)
Future Directions:
Depending on the results of this initial study, future research could explore:
Long-term safety and efficacy Effects on different populations (e.g., varying age groups, ethnicities) Potential interactions with medications or medical conditions Optimal dosing and timing of administration Physiological mechanisms of action
Conclusion:
The Nutraceutical Safety and Efficacy Study represents a rigorous approach to evaluating a novel intervention for mitigating the effects of alcohol overconsumption. By employing a triple-blind, randomized, placebo-controlled design with multiple outcome measures, this study aims to provide robust evidence regarding the safety and efficacy. The results could have significant implications for public health strategies related to alcohol consumption and its associated risks.
Conditions
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Alcohol Consumption
Alcohol
Hangover Symptoms, NAC
Veisalgia
Keywords
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alcohol
blood alcohol
alcohol intoxication
alcohol impairment
BAC
BAC reduction
alcohol half-life
blood alcohol concentration
veisalgia
hangover
Study Design
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Allocation Method
RANDOMIZED
Intervention Model
CROSSOVER
Primary Study Purpose
TREATMENT
Blinding Strategy
QUADRUPLE
Participants
Caregivers
Investigators
Outcome Assessors
Study Groups
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Placebo
Group Type
PLACEBO_COMPARATOR
Placebo
Intervention Type
DIETARY_SUPPLEMENT
Placebo
Liquid
Group Type
ACTIVE_COMPARATOR
Supplement
Intervention Type
DIETARY_SUPPLEMENT
Contains ingredients believed to reduce Blood Alcohol Concentration and symptoms of alcohol impairment.
Interventions
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Supplement
Contains ingredients believed to reduce Blood Alcohol Concentration and symptoms of alcohol impairment.
Intervention Type
DIETARY_SUPPLEMENT
Placebo
Placebo
Intervention Type
DIETARY_SUPPLEMENT
Eligibility Criteria
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Inclusion Criteria
* Over age 21
* Provide signed Informed Consent form electronically in advance of the first study date.
* Provided signed Acknowledgement Form of what is required as part of the study, including use of Uber for transportation to and from each session.
* Not taking certain prescription medications to be listed.
* No history of alcohol or substance abuse issues or alcohol-related medical conditions.
* No history of liver disease.
* No history of significant violent behavior.
* Uses alcohol socially on a regular basis.
* Not naïve to consuming more than 4 drinks at one time.
* Not pregnant or at risk for being pregnant.
* Able to attend all three session dates.
* Own smartphone with text messaging abilities.
* Provide signed Informed Consent form electronically in advance of the first study date.
* Provided signed Acknowledgement Form of what is required as part of the study, including use of Uber for transportation to and from each session.
* Not taking certain prescription medications to be listed.
* No history of alcohol or substance abuse issues or alcohol-related medical conditions.
* No history of liver disease.
* No history of significant violent behavior.
* Uses alcohol socially on a regular basis.
* Not naïve to consuming more than 4 drinks at one time.
* Not pregnant or at risk for being pregnant.
* Able to attend all three session dates.
* Own smartphone with text messaging abilities.
Exclusion Criteria
* Score consistent with Alcohol Use Disorder on the Alcohol Use Disorder Identification Test (AUDIT) a 10 question self-report tool developed by the World Health Organization (WHO).
* Ongoing or regular use of any of the following medications for medical conditions: Antabuse (disulfiram): (Slows alcohol metabolism by inhibiting the elimination of acetaldehyde), Beta-lactam antibiotics: (Some, such as cefmandole, cefoperazone, and moxalactam, can cause a disulfiram-like reaction when alcohol is consumed), Nitrates (Can cause a disulfiram-like reaction when alcohol is consumed), Sulfonylureas (Longer acting ones, such as chlorpropamide and tolbutamide, can cause a disulfiram-like reaction when alcohol is consumed, as well as Pyrazoles and isobutyramide, Inhibit ADH, which decreases the rate at which alcohol is eliminated.)
* Current use of medications likely to be synergistic with one-time excessive use of alcohol: opioids, benzodiazepines, anti-histamines.
* Current use of psychoactive products such as delta 8 or delta 9 tetrahydrocannabinol (THC), Kava, Kratom or psychedelic mushroom (psilocybin).
* Current use of any illegal drug or substance, that includes, but is not limited to -cocaine, methamphetamine, MDMA (ecstasy, molly).
* Active medical conditions that would preclude one-time excessive use of alcohol: Liver disease, diabetes mellitus, seizure disorder/epilepsy, uncontrolled hypertension, cardiac arrhythmia, Multiple Sclerosis, Schizophrenia, Traumatic Brain Injury (TBI), active peptic ulcer disease (PUD), and opioid use disorder
* Ongoing or regular use of any of the following medications for medical conditions: Antabuse (disulfiram): (Slows alcohol metabolism by inhibiting the elimination of acetaldehyde), Beta-lactam antibiotics: (Some, such as cefmandole, cefoperazone, and moxalactam, can cause a disulfiram-like reaction when alcohol is consumed), Nitrates (Can cause a disulfiram-like reaction when alcohol is consumed), Sulfonylureas (Longer acting ones, such as chlorpropamide and tolbutamide, can cause a disulfiram-like reaction when alcohol is consumed, as well as Pyrazoles and isobutyramide, Inhibit ADH, which decreases the rate at which alcohol is eliminated.)
* Current use of medications likely to be synergistic with one-time excessive use of alcohol: opioids, benzodiazepines, anti-histamines.
* Current use of psychoactive products such as delta 8 or delta 9 tetrahydrocannabinol (THC), Kava, Kratom or psychedelic mushroom (psilocybin).
* Current use of any illegal drug or substance, that includes, but is not limited to -cocaine, methamphetamine, MDMA (ecstasy, molly).
* Active medical conditions that would preclude one-time excessive use of alcohol: Liver disease, diabetes mellitus, seizure disorder/epilepsy, uncontrolled hypertension, cardiac arrhythmia, Multiple Sclerosis, Schizophrenia, Traumatic Brain Injury (TBI), active peptic ulcer disease (PUD), and opioid use disorder
Minimum Eligible Age
21 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
Yes
Sponsors
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Medical Life Care Planners, LLC
OTHER
Sponsor Role
lead
Responsible Party
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Gregory L Smith, MD, MPH
Primary Investigator
Responsibility Role
PRINCIPAL_INVESTIGATOR
Principal Investigators
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Gregory L Smith, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
NeX Therapeutics
Locations
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The Warehouse St. Pete
St. Petersburg, Florida, United States
Site Status
Countries
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United States
Central Contacts
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Facility Contacts
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Role: primary
Rachel Borch
Role: backup
Other Identifiers
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000011
Identifier Type: -
Identifier Source: org_study_id