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Effekte von oraler Cortisol oder Propranolol-Gabe auf die Verarbeitung alkoholbezogener Schlüsselreize, den Schlaf und das Rückfallrisiko von alkoholabhängigen Patienten (Copro-Studie). - Copro-Studie

Effekte von oraler Cortisol oder Propranolol-Gabe auf die Verarbeitung alkoholbezogener Schlüsselreize, den Schlaf und das Rückfallrisiko von alkoholabhängigen Patienten (Copro-Studie). - Copro-Studie

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2009-014532-37-DE
Enrollment
Unknown
Registered
2010-10-05
Start date
2011-01-13
Completion date
Unknown
Last updated
2012-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

alkohol dependence

Interventions

Trade Name: Hydrocortison 10 mg Jenapharm Product Name: Hydrocortison 10 mg Jenapharm Pharmaceutical Form: Over encapsulated tablet Pharmaceutical form of the placebo: Capsule* Route of administration

Sponsors

Universitätsklinikum Schleswig-Holstein
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: alcohol dependence, abstention for 3 das minimum before entering the study, male subject, age in the rage 18 to 55 years Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: relevant psychiatric or organic comorbidities that might influence outcome and that might be negatively influenced by study medication e.g. depression, schizophrenia, obsessive comlusive disorder, anorexia, anxiety disorder, dementia, liver-cirrhosis, heart failure, epilepsy, dependence from other legal or illicit drugs.

Design outcomes

Primary

MeasureTime frame
Main Objective: Improvement of the success of cue-exposure by administration of hydrocortisone or propranolol, i.e. stronger attenuation of craving for alcohol;Secondary Objective: 1. improvement of abstination rates 2. testing and improving emotianal memory function 3. improvement of sleep profile 4. normalisation of disturbed cortisol reactivity to stress 5. testing and improving glucose tolerance and insulin resistance;Primary end point(s): ending cue-exposure after 10 sessions maximum, last assesment of sleep and memory in the sleep laboratory after end of cue-exposure treatment.

Countries

Germany

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026