search
Back to results

Brain Imaging Study of the Effects of Modafinil in Cocaine Addiction (CAIMAN)

Primary Purpose

Cocaine Addiction, Cocaine Dependence

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Modafinil and PET (brain imaging)
placebo
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cocaine Addiction focused on measuring Cocaine, Substance abuse, Addiction, Dependence, Modafinil, Brain imaging

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Men of at least 18 years of age
  • Cocaine dependent according to DSM IV TR criteria
  • Seeking treatment
  • Capable of understanding and giving their informed written consent
  • With National Health coverage
  • Urinary screen positive for cocaine in the weeks prior to inclusion

Exclusion Criteria:

  • Women
  • Other DSM IV TR axe I diagnostic criteria (except for tobacco)
  • Neurological disorders
  • Treatment that interferes with the DAT and modafinil
  • Contraindications for modafinil and Magnetic Resonance Imaging

Sites / Locations

  • Unité de recherche U797 Inserm - CEA - Université Paris-Sud. " Neuroimagerie & Psychiatrie " Service Hospitalier Frédéric Joliot
  • Centre d'Enseignement, de Recherche et de Traitements des Addictions - Hopital Universitaire Paul Brousse

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

active

Placebo

Outcomes

Primary Outcome Measures

Decreased DAT occupation rates in the modafinil group versus placebo from day 3 to day of cocaine detoxification.

Secondary Outcome Measures

Evaluation of the clinical efficacy of modafinil during therapeutic cocaine withdrawal.
Correlation between craving measurements, depressive symptom measurements and cognitive deficit measurements observed and modifications of DAT density.
Study of DAT from D3 to D21 versus a pre-existing data base of control subjects.
Tolerance and safety evaluation of high modafinil doses, measured by adverse events and biological parameters.

Full Information

First Posted
June 18, 2008
Last Updated
April 10, 2013
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Mission Interministérielle de Lutte contre la Drogue et la Toxicomanie
search

1. Study Identification

Unique Protocol Identification Number
NCT00701532
Brief Title
Brain Imaging Study of the Effects of Modafinil in Cocaine Addiction
Acronym
CAIMAN
Official Title
Dopamine Transporter (DAT) in Pharmacological Treatments of Cocaine Dependence. CAIMAN (Cocaine Addiction Imaging Medications and Neurotransmitters) Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Completed
Study Start Date
April 2009 (undefined)
Primary Completion Date
October 2012 (Actual)
Study Completion Date
January 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Mission Interministérielle de Lutte contre la Drogue et la Toxicomanie

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
-Context: Study objectives Primary: impact of modafinil versus placebo on DAT density modifications in the striatal and extra-striatal regions in cocaine dependent subjects hospitalised from D3 to D21. Primary Hypothesis: More rapid normalisation of DAT concentrations measured by PET using modafinil versus placebo from D3 to D21 during cocaine detoxification.
Detailed Description
Context: Cocaine dependence is a disorder with a rapidly progressive evolution, associated with various complications. Because of cocaine's direct action on the dopamine transporter (DAT), dopaminergic system dysregulation plays a fundamental role in reinforcement phenomenon and in dependence. This has been proven in numerous animal and post-death human studies of striatal DAT. In vivo studies in cocaine dependent patients are rare. Currently no pharmacotherapy is available to treat this pathology. Current studies indicate that pharmacological agents such as modafinil may be able to reverse the neuroadaptations induced by cocaine dependence. However, no functional neuroimaging study (Positron Emission Tomography, PET) has analysed the impact of medications on DAT density in cocaine dependent patients. However, in primates, in vivo PET has shown modafinil affinity for DAT. Primary Hypothesis: More rapid normalisation of DAT concentrations measured by PET using modafinil versus placebo from D3 to D21 during therapeutic cocaine withdrawal. Study objectives Primary: impact of modafinil versus placebo on DAT density modifications in the striatal and extra-striatal regions in cocaine dependent subjects hospitalised from D3 to D21. Secondary: Evaluation of the clinical efficacy of modafinil during therapeutic cocaine withdrawal. Correlation between craving measurements, depressive symptom measurements and cognitive deficit measurements observed and modifications of DAT density. Study of DAT from D3 to D21 versus a pre-existing data base of control subjects. Tolerance and safety evaluation of high modafinil doses, measured by adverse events and biological parameters. Calculation of the number of subjects: A power of 90% is found for a number of subjects estimated at 24 (bilateral test, α risk at 5%, estimated SEM of 5%, variation of the occupational concentration of the DAT expected to be at least 12% in the modafinil group). Considering the usual rate of patients lost to follow-up in this patient population (25%), we plan to include 30 patients. Methodology: This study is regulated by the law on biomedical research of August 9, 2004. It is a randomised monocentric double blind study versus placebo. During the study, for 90 days, patients will receive in double blind either modafinil or placebo according to their randomisation arm. Evaluations will include 2 PET, cerebral MRI, blood work-up, urinary toxin screen, clinical scales for craving, depression and neuropsychological evaluations. Patients will be recruited over 24 months. The total study length will be 36 months. Primary judgment criteria: Variation of the linking potentials (specific fixation rate for the radioligand [11C]-PE2I to DAT) between the TEP measurement on D3 and D21 within the various anatomical region of interest between the 2 groups (modafinil, placebo). Expected Results: Decreased DAT occupation rates in the modafinil group versus placebo from D3 to D21 of withdrawal.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cocaine Addiction, Cocaine Dependence
Keywords
Cocaine, Substance abuse, Addiction, Dependence, Modafinil, Brain imaging

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
29 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
active
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
Modafinil and PET (brain imaging)
Intervention Description
duration 90 days
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
duration 90 days
Primary Outcome Measure Information:
Title
Decreased DAT occupation rates in the modafinil group versus placebo from day 3 to day of cocaine detoxification.
Time Frame
day 3 and day of cocaine detoxification
Secondary Outcome Measure Information:
Title
Evaluation of the clinical efficacy of modafinil during therapeutic cocaine withdrawal.
Time Frame
D3 to D90
Title
Correlation between craving measurements, depressive symptom measurements and cognitive deficit measurements observed and modifications of DAT density.
Time Frame
D3 to D21
Title
Study of DAT from D3 to D21 versus a pre-existing data base of control subjects.
Time Frame
D3 to D21
Title
Tolerance and safety evaluation of high modafinil doses, measured by adverse events and biological parameters.
Time Frame
D3 to D90

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men of at least 18 years of age Cocaine dependent according to DSM IV TR criteria Seeking treatment Capable of understanding and giving their informed written consent With National Health coverage Urinary screen positive for cocaine in the weeks prior to inclusion Exclusion Criteria: Women Other DSM IV TR axe I diagnostic criteria (except for tobacco) Neurological disorders Treatment that interferes with the DAT and modafinil Contraindications for modafinil and Magnetic Resonance Imaging
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michel Reynaud, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris Hôpital Paul Brousse
Official's Role
Study Director
Facility Information:
Facility Name
Unité de recherche U797 Inserm - CEA - Université Paris-Sud. " Neuroimagerie & Psychiatrie " Service Hospitalier Frédéric Joliot
City
Orsay
ZIP/Postal Code
91401
Country
France
Facility Name
Centre d'Enseignement, de Recherche et de Traitements des Addictions - Hopital Universitaire Paul Brousse
City
Villejuif
ZIP/Postal Code
94800
Country
France

12. IPD Sharing Statement

Learn more about this trial

Brain Imaging Study of the Effects of Modafinil in Cocaine Addiction

We'll reach out to this number within 24 hrs