Effect of Glutathione on Blood Alcohol and Hangover Symptoms

NCT ID: NCT00127309

Last Updated: 2005-08-24

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-06-30

Study Completion Date

2005-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Glutathione (a tripeptide of 3 amino acids - glutamic acid, cysteine and glycine) plays a great role in homeostasis, especially as a potent anti-oxidant.

As an anti-oxidant, it conjugates with xenobiotics using glutathione-S-transferase (GST) and excretes in urine as mercapturic acid.

In 1986, Casciani et al at the University of Milan, studied the effect of glutathione on blood alcohol, acetaldehyde and hepatic triglyceride levels and found a significant reducing effect.

The blood acetaldehyde, which is the metabolic product of ethyl alcohol may have a correlation with hangover symptoms. This study is designed to find this correlation using blood alcohol, blood acetaldehyde levels and the Hangover Symptoms Scale according to the Slutske et al study.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Type of Study: Double-blinded control

Population: 100 males

Inclusion Criteria:

* Males 20-40 years
* Healthy, without chronic diseases, especially must have normal hepatic function, measured by serum SGPT
* No history of alcoholic allergy
* Drink alcohol regularly, at least once a week
* Agree to be a subject by standard consent form

Exclusion Criteria:

* Subject wants to end the study
* Some impending danger to subjects

Number of subjects : 100

Methodology

1. Subjects are recruited;
2. History taking, physical examination and SGPT are done by M.D.;
3. 100 subjects are distributed randomly to numbers 1-100;
4. Factory provides 2 groups of capsules in randomized packets numbered 1 -100; each package contains 3 sub-packages; each sub-package contains 2 capsules of either placebo or 370 mg glutathione capsules. All the three sub-packages will be all placebo or all glutathione. 50 packages are placebo and 50 packages are glutathione;
5. Subjects are examined as follows:

* Hour 0: 3 ml of blood taken for blood alcohol and blood acetaldehyde;
* Hour 0- 1: consume Thai Whisky (40% alcohol) 60 ml with snacks;
* Hour 1: ml of blood taken for blood alcohol and blood acetaldehyde;
* Hour 1.30: ml of blood taken for blood alcohol and blood acetaldehyde;
* Hour 2.30: ml of blood taken for blood alcohol and blood acetaldehyde;
* Hour 3.30: ml of blood taken for blood alcohol and blood acetaldehyde;
* Hour 12: ml of blood taken for blood alcohol and blood acetaldehyde, and Alcohol Hangover Symptom evaluation of each subject is done individually.

Using Wendy S. Slutske et al Scale 0-4:

0= no symptom

1. minimal
2. some
3. much
4. most

Symptoms are

1. extreme thirst or dehydration
2. more tired than usual
3. headache
4. nausea
5. vomiting
6. very weak
7. difficulty concentrating
8. more sensitive to light and sound than usual
9. more sweating than usual
10. have a lot of trouble sleeping
11. anxious
12. depressed
13. trembling or shaking

Blood alcohol, blood acetaldehyde and hangover symptoms are statistically evaluated for significance.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Alcohol Drinking

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

hangover hangover symptoms

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Glutathione

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Healthy
* Males 20-40 years old
* No allergies to alcohol

Exclusion Criteria

* Chronic disease
* Increase in hepatic enzyme SGPT
* Impending danger
Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

T.C Union Global Plc.

UNKNOWN

Sponsor Role collaborator

Piyavate Hospital

OTHER

Sponsor Role lead

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Staporn Jinaratana, M.D

Role: PRINCIPAL_INVESTIGATOR

Piyavate Hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Piyavate Hospital

Bangkok, Bangkok, Thailand

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Thailand

References

Explore related publications, articles, or registry entries linked to this study.

L. Casciani et al.,Effect of GSH on hepatic triglyceride levels at different times after ethanol intoxification IRSC Med.Sci.,vol.14,158(1986)

Reference Type BACKGROUND

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

sj_1

Identifier Type: -

Identifier Source: org_study_id