The Effects of Pharmacotherapy on Brain Mechanisms Underlying Cocaine Dependence.

Sponsor
Hadassah Medical Organization (Other)
Overall Status
Suspended
CT.gov ID
NCT00396734
Collaborator
(none)
40
1
48
0.8

Study Details

Study Description

Brief Summary

The overall aim of this project is to use an advanced brain imaging technique, PET, in order to monitor the progress of pharmacotherapy with modafinil or topiramate for cocaine dependence in methadone-maintained patients who use cocaine in addition. Comparisons will be made within the cocaine dependent methadone maintained subjects, between the start and end of treatment, and between the two medications. This is the first systematic research study of pharmacological treatment for cocaine dependence in Israel. This study is of major clinical use, with implications for the treatment of cocaine dependence in poly-drug abusers in Israel. Successful pharmacotherapy for cocaine dependence is expected in reduction in cue-induced subjective craving and in glucose metabolism in brain areas elicited by cocaine craving. Metabolic activity in regions that are activated by craving should be correlated with dopamine DRD2 receptor occupancy in all patients.

Condition or Disease Intervention/Treatment Phase
  • Drug: Provigil (Modafinil)
  • Drug: Topamax (Topiramate)
N/A

Detailed Description

SPECIFIC AIMS

  1. To try to elucidate the brain mechanisms underlying cocaine dependence and craving in co-morbid cocaine-dependent patients. For this purpose we shall trigger craving for cocaine by exposure to a videotape showing cocaine use and then measure brain metabolic activity using Positron Emission Tomography (PET) and [18F] Fluorodeoxyglucose (FDG)

  2. To evaluate dopamine binding in the brain in the early stage, and at the end of treatment. For this purpose the patients will undergo brain imaging of the dopamine receptor DRD2 by using PET with [11C] raclopride. This is a well established procedure for quantifying the effects of drugs such as amphetamine and cocaine on the brain.

  3. To investigate the association between subjective measures of craving for cocaine and the level of dopamine DRD2 receptor occupancy in the brain.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Effects of Modafinil and Topiramate on Brain Mechanisms Underlying Cue-induced Cocaine Craving and Dependence in Methadone Maintained Cocaine Dependent Patients.
Study Start Date :
Apr 1, 2007
Anticipated Primary Completion Date :
Apr 1, 2011
Anticipated Study Completion Date :
Apr 1, 2011

Outcome Measures

Primary Outcome Measures

  1. Changes in cue-induced brain glucose metabolic activity (FDG) in PET after treatment. [1 month]

  2. Changes in DRD2 receptor density measured by 11 C Raclopride in PET after treatment. [1 month]

  3. Nr.of drug-free urine samples, time to first drug use, duration of longest abstinent period. [1 month]

Secondary Outcome Measures

  1. Craving and psychosocial functioning (e.g., employment status, criminal behavior). [1 month]

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Methadone-maintained cocaine-dependent patients use between 1g to 2g a day; 1 to 3 times a week
Exclusion Criteria:
  • use more than 2g a day; 5 times a week to everyday

  • Subjects who are diagnosed as suffering from psychotic illness according to DSM-IV (Axis 1)22, or with a history of CNS disease, a history of infection that might affect CNS (HIV, syphilis, cytomegalovirus, herpes), or a history of head injury with loss of consciousness,pregnant women.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hadassah Medical Organization Jerusalem Israel 91120

Sponsors and Collaborators

  • Hadassah Medical Organization

Investigators

  • Study Director: Aviv M Weinstein, Ph.D, Hadassah Medical Organization
  • Principal Investigator: Roland Chisin, M.D, Hadassah Medical Organization

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00396734
Other Study ID Numbers:
  • 281006-HMO-CTIL
First Posted:
Nov 7, 2006
Last Update Posted:
Jun 10, 2010
Last Verified:
Jun 1, 2010

Study Results

No Results Posted as of Jun 10, 2010