Steroid Profile: Differentiating Testosterone Administration From (Simultaneous) Ethanol Consumption

NCT ID: NCT04166786

Last Updated: 2019-11-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 4 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-05-06
• Study Completion Date: 2019-09-26

Brief Summary

Background:

Testosterone is an anabolic steroid widely known to improve physical performance. Its consumption is banned by the World Anti-Doping Agency (WADA). The steroid profile is one of the components of the Athlete's Biological Passport (ABP), which consists of selected biological variables that indirectly reveal the effects of doping. Alcohol consumption has been proved to alter the steroid profile and this may lead to the use of ethanol as a masking agent for testosterone administration.

Hypothesis:

Ratios of different testosterone biomarkers vary after ethanol administration: [6-hydroxy-androsterone-3-glucuronide (6OH-Andros3G) / epitestosterone-glucuronide (EG)] and [6-hydroxy-etiocholanolone-3-glucuronide (6OH-Etio3G) / EG] decrease, while [testosterone-glucuronide (TG) / EG] increases.

Primary objective:

To evaluate if the combination of the markers TG, EG, 6OH-Andros3G and 6OH-Etio3G, as well as ethyl glucuronide (EtG) and ethyl sulfate (EtS), can be routinely used to differentiate between changes in the steroid profile due exclusively to the consumption of alcohol and those produced when alcohol is consumed during a testosterone administration.

Secondary objectives:

1. To explore the potential of the simultaneous determination of both phase I and phase II metabolites in alternative matrices (plasma from blood samples collected as for the haematological module of ABP, or saliva) in the screening of testosterone misuse.

2. To look for the differences into a comprehensive steroid profile (determined in urine, plasma and saliva) between samples collected after testosterone administration and after the combination of testosterone and ethanol.

Methods:

Phase I, single-blind, crossover-design clinical trial, placebo controlled, with 4 conditions randomly assigned in male healthy caucasian subjects with a wash-out period between treatments.

Conditions

Healthy Volunteers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: OTHER
• Blinding Strategy: SINGLE

Study Groups

Testosterone + Ethanol

Subjects receive a 3-day treatment with testosterone in combination with ethanol consumption. Subjects have to collect urine in different fractions until 48h post-administration. Blood and saliva samples are also obtained.

Group Type: EXPERIMENTAL

Testosterone gel

Intervention Type: DRUG

Subjects receive a daily transdermal dose of 100 mg of testosterone (2 sachets of 5 g of gel) during 3 days.

Ethanol Solution

Intervention Type: DRUG

Subjects receive a daily administration of 30 g of ethanol (94 mL of Vodka Absolut® diluted in 300 mL of lemon-flavoured water Fontvella®) during 3 days.

Testosterone placebo + Ethanol

Subjects receive a 3-day treatment with testosterone placebo (vaseline) in combination with ethanol consumption. Subjects have to collect urine in different fractions until 48h post-administration. Blood and saliva samples are also obtained.

Group Type: OTHER

Ethanol Solution

Intervention Type: DRUG

Subjects receive a daily administration of 30 g of ethanol (94 mL of Vodka Absolut® diluted in 300 mL of lemon-flavoured water Fontvella®) during 3 days.

Testosterone placebo (vaseline)

Intervention Type: DRUG

Subjects receive a daily transdermal dose of 5 g of pure vaseline ointment during 3 days.

Testosterone + Ethanol placebo

Subjects receive a 3-day treatment with testosterone in combination with ethanol placebo (lemon-flavoured water). Subjects have to collect urine in different fractions until 48h post-administration. Blood and saliva samples are also obtained.

Group Type: OTHER

Testosterone gel

Intervention Type: DRUG

Subjects receive a daily transdermal dose of 100 mg of testosterone (2 sachets of 5 g of gel) during 3 days.

Ethanol placebo (lemon-flavoured water)

Intervention Type: DRUG

Subjects receive a daily administration of 394 mL of lemon-flavored-water Fontvella® during 3 days.

Testosterone placebo + Ethanol placebo

Subjects receive a 3-day treatment with testosterone placebo (vaseline) in combination with ethanol placebo (lemon-flavoured water). Subjects have to collect urine in different fractions until 48h post-administration. Blood and saliva samples are also obtained.

Group Type: PLACEBO_COMPARATOR

Testosterone placebo (vaseline)

Intervention Type: DRUG

Subjects receive a daily transdermal dose of 5 g of pure vaseline ointment during 3 days.

Ethanol placebo (lemon-flavoured water)

Intervention Type: DRUG

Subjects receive a daily administration of 394 mL of lemon-flavored-water Fontvella® during 3 days.

Interventions

Testosterone gel

Subjects receive a daily transdermal dose of 100 mg of testosterone (2 sachets of 5 g of gel) during 3 days.

Intervention Type: DRUG

Ethanol Solution

Subjects receive a daily administration of 30 g of ethanol (94 mL of Vodka Absolut® diluted in 300 mL of lemon-flavoured water Fontvella®) during 3 days.

Intervention Type: DRUG

Testosterone placebo (vaseline)

Subjects receive a daily transdermal dose of 5 g of pure vaseline ointment during 3 days.

Intervention Type: DRUG

Ethanol placebo (lemon-flavoured water)

Subjects receive a daily administration of 394 mL of lemon-flavored-water Fontvella® during 3 days.

Intervention Type: DRUG

Other Intervention Names

Testogel 50 mg®; Vodka Absolut®; Vaselina Pura Pege®; Lemon flavored-water Fontvella®

Eligibility Criteria

Inclusion Criteria

• Healthy Caucasian men aged 18 to 40 years.
• Clinical history and physical examination demonstrating no organic or psychiatric disorders.
• The ECG and general blood and urine laboratory tests performed before the study should be within normal ranges. Minor or occasional changes from normal ranges are accepted if, in the investigator's opinion, considering the current state of the art, they are not clinically significant, are not life-threatening for the subjects and do not interfere with the product assessment. These changes and their non-relevance will be justified in writing specifically.
• The body mass index (BMI=weigh/height2) will range from 19 to 27 kg/m2, and the weight from 50 to 100 kg.
• Understanding and accepting the study procedures and signing the informed consent.
• Agreeing to follow a diet free from ethanol in the 72 hours prior to the start of each session and until the end of the study.
• Subjects with social or recreational alcohol consumption, at least 3 Standard Drink/week and subjects with experience in several drunkenness.
• Volunteers with normal steroidal profile for Caucasian population (0.7 ≤T / E ≤3)

• Allergy, idiosyncrasy, hypersensitivity or adverse reactions to the active substance of Testogel gel®, which is synthesized from soy, or to any of the excipients or to vaseline ointment.
• Subjects with intolerance or adverse reactions to ethanol.
• History or clinical evidence of alcoholism, drug abuse, or regular use of psychoactive drugs.
• History or clinical evidence of cardiovascular, respiratory, renal, hepatic, endocrine, gastrointestinal, hematological, neurological, dermatological or other acute or chronic diseases that, in the opinion of the Principal Investigator or the collaborators designated by it, may pose a risk to the subjects or interfere with the objectives of the study. Especially history of epilepsy and migraine, edema, hypertension, diabetes mellitus, hypercalcemia or polyglobulia.
• History of psychiatric disorders.
• History or clinical evidence of gastrointestinal, liver, renal or other disorders which may lead to suspecting a disorder in drug absorption, distribution, metabolism or excretion, or that suggest gastrointestinal irritation due to drugs.
• Subjects with contraindications to treatment with the study drugs (according to the respective technical data sheets). Especially a history of breast cancer, liver cancer, suspicion or confirmation of prostate carcinoma Subjects and subjects who have suffered a hospitalization caused by alcohol intoxication or who have received treatment for drunkenness
• Having suffered any organic disease or major surgery in the three months prior to the study start.
• Symptoms compatible with a prostatic syndrome: increase in the number of urinations, difficulty to initiate urination, thinner and less potent urine stream, urination in several times, incomplete emptying of urine feeling.
• Prostate-specific antigen (PSA) values outside the normal range for the volunteer's age.
• Subjects with positive serology to Hepatitis B, C or HIV.
• Presence of bacterial, fungal or deep cuts in the area of skin chosen for cutaneous applications.
• Regular use of any drug in the month prior to the study sessions. The treatment with single or limited doses of symptomatic medicinal products in the week prior to the study sessions will not be a reason for exclusion if it is calculated that it has been cleared completely the day of the experimental session.
• Blood donation 8 weeks before or participation in other clinical trials with drugs in the previous 12 weeks.
• Smokers of more than 20 cigarettes per day.
• Taking more than 40 g of alcohol a day
• Consumers of more than 5 coffees, teas, cola drinks, or other stimulant drinks or with xanthines daily in the 3 months prior to the start of the study.
• Ingestion of vitamin supplements or antioxidants or Non-Steroidal Anti-Inflammatory Drugs (NSAID) in the two weeks preceding the study.
• Subjects unable to understand the nature, consequences of the study and the procedures requested to be followed.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Parc de Salut Mar

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ana M Aldea Perona, Dr

Role: PRINCIPAL_INVESTIGATOR

IMIM (Hospital del Mar Medical Research Institute)

Locations

IMIM (Hospital del Mar Medical Research Institute)

Barcelona, , Spain

Countries

Spain

Other Identifiers

IMIMFTCL/SPOL/1

Identifier Type: -

Identifier Source: org_study_id