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Effects of Glucocorticoids on Craving During Detoxification Treatment of Heroin and/or Stimulants

Effects of Glucocorticoids on Craving During Detoxification Treatment of Heroin and/or Stimulants

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02935101
Acronym
Goliath
Enrollment
4
Registered
2016-10-17
Start date
2016-10-31
Completion date
2017-05-31
Last updated
2019-05-23

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

Conditions

Cocaine Dependence, Opioid Dependence

Keywords

glucocorticoids, craving, Heroin, Cocaine, dependency

Brief summary

The purpose of this study is to evaluate whether prednisolone lowers intensity and frequency of craving in heroin-addicted subjects undertaking a detoxification of cocaine and/or heroin.

Detailed description

Participants of this study are 120 heroin-addicted patients who are inward for a detoxification program for either cocaine or cocaine and heroin. Depending on the detoxification substance(s) there will be two groups of participants: Detoxification of cocaine (A; 60 participants) and detoxification of heroin and cocaine (B; 60 participants). The detoxification starts mandatory with the admission to the ward and lasts about 1-2 weeks. The participation in the study lasts about 4-5 weeks (including follow-up visits). Intake of study medication starts two days after admission and one day after informed consent. Each participant will get either 30mg/d prednisolon or placebo during five days. Participants will be under normal medical supervision during the treatment phase until follow-up 2 (final examination) provided by ward staff. Treatment days and follow-up 1 and 2 consist of : (1) vital signs (BP, HR, temperature) as measured in the daily routine, (2) at midday: visual analogue scales asking about craving for heroin and cocaine at the moment, (3) afternoon: questionnaires to survey mainly the withdrawal symptoms and vegetative parameters.

Interventions

DRUGPrednisolone

formulated for oral administration. encapsulated.

DRUGPlacebo (for Prednisolone)

Sugar pill manufactured to mimic Prednisolon 10mg capsules

Sponsors

Psychiatric Hospital of the University of Basel
CollaboratorOTHER
Prof. Dominique de Quervain, MD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Informed Consent as documented by signature, * age ≥18, * Group A Detoxification of stimulants (cocaine, amphetamine and/or methamphetamine); ICD-10: F14.2 and/or F15.2) OR Stable opioid dependency (no parallel consumption). Detoxifica-tion of stimulants. * Group B Opioid dependency and dependency of stimulants (cocaine, amphetamine and/or methamphetamine) and Detoxification of parallel consumption of stimulants and heroin (ICD-10: F11.2, 14.2, 15.2) * admission for detoxification to ward U2 of the University Psychiatric Hospital of Basel

Exclusion criteria

* contraindications to the class of drugs under study or to any of the excipients, e.g. known hypersensitivity or allergy to class of drugs or the investigational product; * acute or severe co-morbid psychiatric disturbances (such as a heavy episode of major depression with suicidal ideations, acute exacerbation of a bipolar disorder, acute exacerbation of schizophrenia, alcohol addiction with an acute relapse, psychosis, dementia); * current medical conditions excluding participation (such as acute infectious disease, moni-tored by elevated CRP, diabetes mellitus, anticoagulation therapy); * recent history of systemic or topic glucocorticoid therapy; * alcohol intake \> 0.0 ‰ according to breathalyser test on day 0 (screening) to exclude severe alcohol abuse; * specific drugs not allowed during the study or for specific periods of time prior to the administration of the test dose: Anticoagulant agents, antidiabetic agents, cyclosporine; * women who are pregnant or breast feeding; * intention to become pregnant during the course of the study; * inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia; * participation in another study with investigational drug within the 30 days preceding or during the present study; * previous enrolment into the current study; * enrolment of the investigator, his/her family members, employees and other dependent persons.

Design outcomes

Primary

MeasureTime frameDescription
Heroin CravingAssessing change between baseline and some predefined time points during 2 weeksHeroin Craving Questionnaire, 14 items (HCQ; Tiffany et al., 1993 and Heinz et al., 2006)
Cocaine CravingAssessing change between baseline and some predefined time points during 2 weeksCocaine Craving Questionnaire, 14 items (CCQ; Tiffany et al., 1993 and Heinz et al., 2006)

Secondary

MeasureTime frameDescription
Questionnaire 'Anger/Irritation'Assessing change between baseline and some predefined time points during 2 weeksSTAI-G form X1 (state; Laux L. et al., 1981)
Withdrawal Symptoms according to ICD-10 (F14.3 and F12.2)Assessing change between baseline and some predefined time points during 2 weeks
Saliva Cortisol levelsAssessing change between baseline and some predefined time points during 2 weeks
Questionnaire 'Anxiety'Assessing change between baseline and some predefined time points during 2 weeksSTAXI (Schwenkmezger P. et al., 1992/2006)
Questionnaire 'Health State'Assessing change between baseline and some predefined time points during 2 weeksSF-12 (Morfeld M. et al., 2011)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026