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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03892369
Other study ID # H-18063495
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2019
Est. completion date September 1, 2021

Study information

Verified date December 2021
Source University Hospital, Gentofte, Copenhagen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Plasma fibroblast growthfactor-21 (FGF21) responses to acute alcohol exposure will be evaluated in three groups: A: 15 individuals diagnosed with alcohol dependence (ICD10 code F10.2) and no alcoholic liver diseases, B: 15 healthy individuals with one or two parents with alcohol dependence, and C: 15 healthy matched controls without history of or disposition to alcohol dependence. The experimental day consists of a load of 0.5 g ethanol per kg body weight ingested from time 0-10 minutes followed by a 7 h period in which blood will be sampled with frequent intervals, rating of preference for ethanol, salt, sour, bitterly and sweets, sensations of hunger, appetite, satiety, headache, and nausea will be evaluated using visuel analogue scale and resting energy expenditure will be evaluated using indirect calorimetry.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date September 1, 2021
Est. primary completion date June 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 25 Years to 65 Years
Eligibility Inclusion Criteria: - Informed consent - Caucasian males between 25 and 65 years of age - BMI between 19 and 27 kg/m2 - Normal haemoglobin - Normal fasting plasma glucose concentration (< 6 mmol/l) and normal glycated haemoglobin A1c (HbA1c) (< 42 mmol/mol) Participants with a father diagnosed with alcohol dependence (group B): - Father diagnosed with alcohol dependence - Weekly alcohol intake of less than 14 units of alcohol (of 12 g) - Normal Alcohol Use Disorders Identification Test (AUDIT) score Healthy participants (group C): - Weekly alcohol intake of less than 14 units of alcohol (of 12 g) - Normal AUDIT score Exclusion Criteria: - Liver disease evaluated by plasma alanine aminotransferase (ALAT) > 3 × normal level, an international normalised ratio (INR) below normal values, or biopsy-verified alcoholic liver disease - Diabetes mellitus - Anaemia - Nephropathy - Other diseases the investigator finds disruptive for participation in the study. Participants with a father diagnosed with alcohol dependence (group B): - Former alcohol dependence or abuse Healthy participants (group C): - First-degree relatives with diabetes, liver disease and/or alcohol dependence - Former alcohol dependence

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Ethanol
Ethanol administration

Locations

Country Name City State
Denmark Center for Clinical Metabolic Research, Gentofte Hospital Hellerup

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Gentofte, Copenhagen

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fibroblast growthfactor-21 Plasma FGF21 concentrations, a member of the endocrine FGF-family One year
Secondary Ethanol Plasma ethanol concentration One year
Secondary Glucose Plasma glucose concentrations One year
Secondary Insulin and C-peptide Serum insulin and C-peptide concentrations One year
Secondary Glucagon Plasma glucagon concentration One year
Secondary Tumor Necrosis Factor-alpha (TNF) Plasma TNF-alpha concentrations One year
Secondary Lipopolysaccharide Binding Protein (LBP) Plasma LBP concentrations One year
Secondary Interferon-gamma (INF) Plasma INF-gamma concentrations One year
Secondary Interleukine-10 (IL-10) Plasma IL-10 concentrations One year
Secondary Interleukine-8 (IL-8) Plasma IL-8 concentrations One year
Secondary Interleukine-6 (IL-6) Plasma IL-6 concentrations One year
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