Validation of a Test System for Development of Medications for Alcoholism

Alcoholism Clinical Trial

— TEMANX  

Official title:

Validation of a Test System for Development of Medications for Alcoholism

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02652585
• Other study ID #: TUD-TEMANX-065
• Status: Completed
• Phase: Phase 3
• First received: January 6, 2016
• Last updated: September 26, 2017
• Start date: February 2016
• Est. completion date: September 4, 2017

Study information

• Verified date: September 2017
• Source: Technische Universität Dresden
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Using theTEMA (test system for development of medications for alcoholism) it can be shown, that naltrexone administration reduces the willingness to perform work for alcohol infusion in a laboratory experiment.

Description:

Objective of this study is to show that a laboratory alcohol self-administration method can predict the therapeutic potential of new compounds to reduce relapse in alcohol-dependent patients.

The 'TEMA" translates several animal behavioral paradigms of alcohol self-administration into corresponding human experiments.

We will investigate the opiate antagonist Naltrexone, whose anti-relapse effect is well documented, as a reference drug for validation.

Main objective:

With TEMA (test system for development of medications for alcoholism ) it can be shown, that naltrexone administration reduces the willingness to perform work for alcohol infusion in a laboratory experiment.

Secondary objectives:

• administration of naltrexone in comparison to placebo leads to a reduction of alcohol craving and real-life drinking

• administration of naltrexone in comparison to placebo leads to reduction of the CDT-Level

• administration of naltrexone in comparison to placebo leads to a change in perception of subjective alcohol effects

• the effectiveness of naltrexone can be predicted by the A118G polymorphism of the OPRM1

• administration of naltrexone changes the baseline and alcohol-induced ability of motor inhibition

• administration of naltrexone changes the baseline and alcohol-induced regional cerebral perfusion

• administration of naltrexone changes the baseline and alcohol-induced cerebral resting state activity

• changes of alcohol effects to the brain activity induced by naltrexone in comparison to placebo correlate with effects of naltrexone on the willingness to work for alcohol self-administration

Recruitment information / eligibility

• Status: Completed
• Enrollment: 46
• Est. completion date: September 4, 2017
• Est. primary completion date: August 25, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 25 Years to 55 Years

Eligibility

Inclusion Criteria:

• male and female volunteers aged 25 to 55 years

• at least weekly alcohol consumption at a medium risk level according to WHO in the Timeline Follow-back Interview over the last 45 day with an average amount of alcohol of 41 g/day (men) or 31 g/day (women)

• at least 6 days with an alcohol consumption of >100 g/day (men) or 75 g/day (women) and at least 4 non consecutive alcohol abstinent days in the last 45 days

• at least 1 drinking day in each full week between screening and visit 1 and not more than 6 abstinent days in the week before visit 1

• no demand of treatment of the risky alcohol consumption

• written consent after Information

Exclusion Criteria:

• a history of hypersensitivity against alcohol or one of the used medicinal products, of their ingredients or medicinal products with similar chemical structures

• participation in another clinical trial within the last 4 weeks before inclusion

• addiction or other disorders, which will not allow the subject to assess the character and importance or possible consequences of the clinical trial

• pregnant or breastfeeding women

• women capable of bearing children, except women who fulfil following criteria:- post-menopausal (12 months natural amenorrhoea or 6 month amenorrhoea and Serum FSH >40 ml U/ml) - post operative (6 weeks after ovariectomy on both sides with or without hysterectomy) - regular and correct use of a contraceptive method with an error Quote of < 1 % per year (for example implants, depot injections, oral contraceptive, IUP). It has to be recognized that a combined oral contraception - in contrast to pure progesterone compounds - have a failure rate of < 1 %. Hormone IUDs with a Pearl Index of 1 % are safer than copper IUDs. - sexual abstinence - vasectomy of the Partner

• evidence that the participant is not expected to comply with the protocol (for example lacking compliance)

• current or previous alcohol or substance dependence according to DSM-IV (exception:

tobacco dependence)

• current or previous treatment because of alcohol, for example in an addiction advisory cen-tre, self-help group, detoxification treatment

• current or previous diseases, where an alcohol infusion can cause a clinically relevant hazard (e. g. pancreatitis, liver cirrhosis)

• current or planned intake of opiate analgesics

• current psychiatric treatment or intake of psychiatric drug or suffering from of a psychiatric disease requiring treatment

• a history of suicide attempt

• CIWA-Score >5 at Screening (alcohol withdrawal scale)

• a history of symptoms of alcohol withdrawal, epileptic seizures or delirium

• routine laboratory Parameters, indicating relevant liver-, pancreas- or kidney injury, an acute infection, anaemia or lack of vitamins (ASAT, ALAT > twofold of the standard at screening, gamma-GT, lipase >threefold of the standard, CRP < 15 mg/l, creatin indicating a moderate renal insufficiency ( eGFR <60 ml/min), leucocytes > 12000/µl, haemoglobin < 7,5 mmol/l (men) or 6,5 mmol/l (women), MCV > 100 fl)

• Body weight > 130 kg

• drug screening in urine: once positive at screening for opiate, cannabis, cocaine, amphetamines, benzodiazepines or positive once at visit 1 for opiates or positive twice at visit 1 for cannabis, cocaine, amphetamines, benzodiazepines

• breath alcohol concentration at screening once > 0,00 g/kg or twice >0,00 g/kg at visit 1

• unsuitable for fMRT (e. g. cardiac pacemaker, claustrophobia)

• specific contraindications against naltrexone: o acute hepatitis o severe or acute liver disease o severe kidney disease o rare hereditary galactose intolerance, Lapp-lactase-deficiency or Glucose-galactose-malabsorption

Related Conditions & MeSH terms

• Alcoholism

Intervention

Drug:
• Naltrexone

• Placebo
capsule filled with micro crystalline cellulose, manufactured to mimic naltrexone capsule

Locations

Country	Name	City	State
Germany	Klinik und Poliklinik für Psychiatrie und Psychotherapie	Dresden

Sponsors (1)

Lead Sponsor	Collaborator
Technische Universität Dresden

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Difference CAT Trials alcohol	Difference of cumulative number of work sets for alcohol in the "constant attention task" between first measurement (without medication) and second measurement (with medication)	one year
Secondary	Difference CAT Trials sodium chloride solution	Difference of cumulative number of work sets for sodium chloride solution in the "constant attention task" between first measurement (without medication) and second measurement (with medication)	one year
Secondary	break Point alcohol	Difference of the "break point" in the "progressive work" schedule for the work for alcohol between first measurement (without medication) and second measurement (with medication). The "break point" is the number of the last alcohol request before subjects stop to work for more alcohol.	one year
Secondary	max. BAC	Maximal achieved blood alcohol concentration (BAC) in alcohol self-administration between first measurement (without medication) and second measurement (with medication)	one year
Secondary	Drinking habits	Drinking habits measured with Timeline Follow-back Interview over 45 days before study start (measured at screening) and over the entire study duration (between screening and the last day of medicinal product intake, ascertained at visit 5): drinking days, amount of alcohol per drinking day and number of days with alcohol consumption over 60 g (men) or 48 g (women)	one year
Secondary	CDT - level	CDT - level: (carbohydrate-deficient transferrin), measured at visit 1 and visit 5	one year
Secondary	alcohol craving	Alcohol craving in daily routine (OCD - scale) measured at visit 1 and visit 4	one year
Secondary	subjective alcohol effects	Difference in subjective alcohol effects between first measurement (without medication) and second measurement (with medication), measured with visual analogue scales ("Quizzer") before, during and after the alcohol infusion	one year
Secondary	motor impulse control	Capacity for motor impulse control during infusion of physiologic saline solution or alcohol as NIMPs (single-blinded), measured with the counting stroop task (in Verum and placebo group) at visit 3 and 4	one year
Secondary	cerebral blood flow (CBF)	Regional cerebral perfusion in ml/100 g tissue per Minute during infusion of sodium chloride solution or alcohol as NIMPs (single-blinded), measured with arterial spin labeling (ASL) under verum or placebo condition at visit 3 and 4	one year
Secondary	Cerebral resting state activity	Cerebral resting state activity during infusion of sodium chloride solution or alcohol as NIMPs (single-blinded), measured with BOLD fMRI (in Verum and placebo group) at visit 3 and 4	one year
Secondary	adverse events	Medical survey concerning occurring adverse events at visit 1 to 5	one year
Secondary	ALAT	ALAT (alanine aminotransferase) in µmol/ s*l before inclusion (screening visit), at visit 4 and after finishing all study relating interventions (visit 5)	one year
Secondary	ASAT	ASAT (aspartate aminotransferase) in µmol/ s*l before inclusion (screening visit), at visit 4 and after finishing all study relating interventions (visit 5)	one year
Secondary	Gamma-GT	Gamma-GT in µmol/ s*l before inclusion (screening visit) and after finishing all study relating interventions (visit 5)	one year
Secondary	standard blood cell count	standard blood cell count before inclusion (screening visit), at visit 4 and after finishing all study relating interventions (visit 5)	one year
Secondary	creatinine	creatinine in µmol/l before inclusion (screening visit)	one year
Secondary	lipase	lipase in µmol/ s*l before inclusion (screening visit) and after finishing all study relating interventions (visit 5)	one year
Secondary	CRP	CRP (C-reactive protein) in mg / l before inclusion (screening visit) and after finishing all study relating interventions (visit 5)	one year