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Relationship Between D2 Receptors SPECT and the Apomorphine Test in Patients With OH Dependence (ALC-DRD2-APO)
This study is currently recruiting participants.
Verified by Hospital University Vall d'Hebron, June 2008
Sponsored by: Hospital University Vall d'Hebron
Information provided by: Hospital University Vall d'Hebron
ClinicalTrials.gov Identifier: NCT00437177
  Purpose

OH dependence is associated with DA receptor changes. Both, the apomorphine test and the D2Rec SPECt are usefull for monitoring DA receptor status. We aimed at studying whether DA receptor hypofunction, assessed by means of the apomorphine test and the D2Rec SPECT, is a marker of relapse in detoxified OH dependents patients.


Condition Intervention Phase
Alcoholism
Drug: apomorphine
Drug: [(123)I] iodobenzamide
Phase II

MedlinePlus related topics: Alcoholism
Drug Information available for: Apomorphine hydrochloride Apomorphine
U.S. FDA Resources
Study Type: Interventional
Study Design: Basic Science, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment
Official Title: Relationship Between D2 Receptors SPECT and the Apomorphine Test in Patients With OH Dependence: Predictive Value for Relapse

Further study details as provided by Hospital University Vall d'Hebron:

Primary Outcome Measures:
  • To detertmine the agreement rate of the dopaminergic sensibility assessed by two different techiniques: the apomorphine test and and IBZM SPECT. [ Time Frame: 3 months ] [ Designated as safety issue: No ]

Estimated Enrollment: 50
Study Start Date: January 2007
Estimated Study Completion Date: December 2008
Estimated Primary Completion Date: December 2008 (Final data collection date for primary outcome measure)
Intervention Details:
    Drug: apomorphine
    Apomorphine 0.05 mg/kg subcutaneously at hospital admission and at discharge. Abstinent participants at 3 months will receive a third dose.
    Drug: [(123)I] iodobenzamide
    [(123)I] iodobenzamide 185 MBq I.V., at discharge.
  Eligibility

Ages Eligible for Study:   25 Years to 60 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • alcohol dependence
  • alcohol dependence length at least 8 years.
  • male
  • age 25 - 60 years

Exclusion Criteria:

  • other drug dependence (except nicotine dependence)
  • another major axis I psychiatric diagnosis
  • comorbid neurological disorder
  • comorbid cardiovascular disorder
  • comorbid metabolic disorder
  • brain injury
  • apomorphine allergy
  • iode allergy
  • diazepam allergy
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00437177

Contacts
Contact: Miquel Casas, Prof. mcasas@vhebron.net
Contact: Xavier Castells, Prof xcc@icf.uab.cat

Locations
Spain, Catalonia
Psychiatry Service, Hospital Universitari Vall d'Hebron Recruiting
Barcelona, Catalonia, Spain, 08036
Contact: Miquel Casas, Prof         mcasas@vhebron.net    
Contact: Xavier Castells         xcc@icf.uab.cat    
Principal Investigator: Miquel Casas, Prof            
Sponsors and Collaborators
Hospital University Vall d'Hebron
Investigators
Principal Investigator: Miquel Casas, Prof Psychiatry Service, Hospital Universitari Vall d'Hebron
  More Information

Responsible Party: Servei de Psiquiatria. Hospital Universitari Vall d'Hebron ( m )
Study ID Numbers: OH SPECT APO, EudraCT: 2004-001893-24
Study First Received: February 16, 2007
Last Updated: June 4, 2008
ClinicalTrials.gov Identifier: NCT00437177  
Health Authority: Spain: Spanish Agency of Medicines

Keywords provided by Hospital University Vall d'Hebron:
alcoholism
apomorphine
iodobenzamide
imaging
spect
relapse

Study placed in the following topic categories:
Dopamine
Mental Disorders
Alcoholism
Substance-Related Disorders
Disorders of Environmental Origin
Alcohol-Related Disorders
Apomorphine

Additional relevant MeSH terms:
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Anti-Dyskinesia Agents
Therapeutic Uses
Physiological Effects of Drugs
Antiparkinson Agents
Dopamine Agents
Dopamine Agonists
Central Nervous System Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 15, 2009