Evaluation of a Fixed Combination of Herbal Extracts to Prevent Symptoms Alcohol-induced Hangovers

NCT04183842 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2019-12-03

No results posted yet for this study

Summary

The primary objective of the study is to test whether the tested Product LACIME Anti-hangover is effective in preventing the signs and symptoms of alcohol-induced hangover (such as headache, impaired memory, depression, anxiety, weakness, trouble sleeping and concentrating, nausea, dizziness, sleepiness, thirsty, dry mouth, sweating, sensitivity to light and sounds, vision problems) in healthy subjects.

Conditions

Interventions

DIETARY_SUPPLEMENT

LACIME Anti-hangover

LACIME Anti-hangover contains the following excipients: * Purified water, * Xanthan gum, * Glycerin, * Potassium sorbate (as a preservative) * Citric acid (acidity regulator) * Aroma (flavouring agent) LACIME Anti-hangover contains the following plant extracts and vitamin: * Curcuma longa rhizome extract (Curcuma), * Panax quinquefolius extract (Ginseng panax), * Malpighia punicifolia extract (Acerola), * Silybum marianum extract (Milk thistle), * Desmodium adscendens extract (Desmodium), * Pyridoxine chlorhydrate (Vitamin B6).

OTHER

Placebo

Placebo contains the following excipients : * Purified water, * Xanthan gum, * Glycerin, * Potassium sorbate (as a preservative) * Citric acid (acidity regulator) * Aroma (flavouring agent) Placebo contains : \- Carrot juice

Sponsors & Collaborators

  • Phytomed AB

    collaborator OTHER
  • Incara Lab

    lead INDUSTRY

Principal Investigators

  • Alexander PANOSSIAN, Pr., Dr · Swedish Herbal Institute AB

  • Areg HOVHANNISYAN, PhD, Dr.Sci · Head od National Anti-Doping Organization

  • Artur POTOSSIAN, Dr. MD · CARDIOMED Family Health Center

  • Samvel HAYRUMYAN, PhD, MD · CARDIOMED Family Health Center

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
CROSSOVER

Eligibility

Min Age
20 Years
Max Age
30 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-07-04
Primary Completion
2019-08-26
Completion
2019-09-07

Countries

  • Armenia

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04183842 on ClinicalTrials.gov