Extended Release Naltrexone for Treating Amphetamine Dependence in Iceland

The recruitment status of this study is unknown because the information has not been verified recently.
Verified April 2010 by National Institute on Drug Abuse (NIDA).
Recruitment status was  Not yet recruiting
Sponsor:
Collaborator:
Society of Alcoholism and other Addictions
Information provided by:
National Institute on Drug Abuse (NIDA)
ClinicalTrials.gov Identifier:
NCT01100853
First received: April 7, 2010
Last updated: April 9, 2010
Last verified: April 2010
  Purpose

Until positive results were found with oral naltrexone, no medication has been effective against amphetamine dependence. The primary aim of this pilot study is to replicate the findings of the Swedish team that showed oral Naltrexone prevented relapse to amphetamine addiction and to extend their results by randomizing treatment-seeking amphetamine addicted patients to a 6 month course of VIVITROL (naltrexone for extended-release injectable suspension) or VIVITROL placebo. Patients in each group will receive drug counseling. VIVITROL is administered monthly and may be a better test of efficacy than tablets that must be taken daily.


Condition Intervention Phase
Amphetamine Dependence
Drug: VIVITROL/VIVITROL placebo injection, 24 weeks
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Extended Release Naltrexone for Treating Amphetamine Dependence in Iceland

Resource links provided by NLM:


Further study details as provided by National Institute on Drug Abuse (NIDA):

Primary Outcome Measures:
  • Between group proportions of Amphetamine negative urine tests. [ Time Frame: 24 Weeks ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Time to relapse: HIV risk behavior; Treatment retention; Amphetamine craving; Use of amphetamine and other drugs; Criminal activity; Depression; Quality of Life [ Time Frame: 24 weeks ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 100
Study Start Date: May 2010
Estimated Study Completion Date: May 2012
Estimated Primary Completion Date: May 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: VIVITROL injection, 24 weeks
Efficacy of 24 week course of VIVITROL with counseling as compared to 24 week course of VIVITROL placebo with counseling (monthly injections)
Drug: VIVITROL/VIVITROL placebo injection, 24 weeks
Efficacy of 24 week course of VIVITROL with counseling as compared to 24 week course of VIVITROL placebo with counseling (monthly injections)
Placebo Comparator: VIVITROL placebo injection, 24 weeks
Efficacy of 24 week course of VIVITROL with counseling as compared to 24 week course of VIVITROL placebo with counseling (monthly injections)
Drug: VIVITROL/VIVITROL placebo injection, 24 weeks
Efficacy of 24 week course of VIVITROL with counseling as compared to 24 week course of VIVITROL placebo with counseling (monthly injections)

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age 18 or above;
  • Diagnosis of amphetamine dependence as defined by DSM-IV-TR with 10 or more days of amphetamine use in the past month, and patient and clinician identify amphetamine dependence as the main problem;
  • Abstinent from substances (alcohol, amphetamines, cannabinoid, cocaine, hallucinogens, opioids, benzodiazepines [unless used to treat alcohol withdrawal] for at least 7 days prior to receiving study drug or placebo;
  • Provision of telephone numbers/contacts of three or more people that are likely to know where can be located if unable to be contacted directly;
  • Successfully complete 7-10 day assessment and study baseline measures at Vogur

Exclusion Criteria:

  • Any liver test >5 times the top limit of normal; Physiologically dependent on opioids or other substances (nicotine excepted) at time of admission to Vogur;
  • Suspected or known concomitant use of opioid analgesics, positive opioid urine drug test or positive naloxone challenge:
  • Schizophrenia, Bipolar I or other non-substance related psychotic disorder; Severely depressed, suicidal or homicidal: Dementia: Inability to understand the informed consent;
  • Planning to move from the Reykjavík area or enter jail within the next 12 months;
  • Likely to receive opioid analgesics in next 6 months associated with possible or scheduled surgery or procedure;
  • Known hypersensitivity to naltrexone, polyactide-co-glycolide (PLG); carboxymethylcellulose, or any other component of the diluent;
  • Female subjects who are pregnant or lactating, or of child bearing potential who are not using acceptable methods of birth control;
  • A body habitus that precludes use of the customized needle for intramuscular injection, based on clinical judgment;
  • Use of an investigational agent in the past 30 days
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01100853

Contacts
Contact: Thorarinn Tyrfingsson, M.D. +354 530 7670 thorarinn@saa.is
Contact: Valgerdur Runarsdottir +354 530 7655 vlgerdurr@saa.is

Locations
Iceland
SAA National Center of Addiction Medicine, Vogur Hospital Not yet recruiting
Storhofoi 45, 110 Reykjavik, Iceland
Contact: Igunn Hansdottir, Ph.D.     +354 530 7602     ingunnh@saa.is    
Contact: Valgerdur Runarsdottir     +354 530 7655     valgerdurr@saa.is    
Principal Investigator: Thorarinn Tyfingsson, M.D.            
Sub-Investigator: Valgerdur Runarsdottir            
Sponsors and Collaborators
Society of Alcoholism and other Addictions
Investigators
Principal Investigator: Helen Pettinati, Ph.D University of Pennsylvania
Principal Investigator: George Woody, M.D. University of Pennsylvania
  More Information

No publications provided

Responsible Party: Helen Pettinati, Ph.D., University of Pennsylvania
ClinicalTrials.gov Identifier: NCT01100853     History of Changes
Other Study ID Numbers: 811095, 2009-013647-10
Study First Received: April 7, 2010
Last Updated: April 9, 2010
Health Authority: United States: Food and Drug Administration

Keywords provided by National Institute on Drug Abuse (NIDA):
amphetamine dependence
amphetamine injection
VIVITROL/VIVITROL placebo
amphetamine craving

Additional relevant MeSH terms:
Amphetamine-Related Disorders
Substance-Related Disorders
Mental Disorders
Amphetamine
Methamphetamine
Naltrexone
Central Nervous System Stimulants
Physiological Effects of Drugs
Pharmacologic Actions
Central Nervous System Agents
Therapeutic Uses
Sympathomimetics
Autonomic Agents
Peripheral Nervous System Agents
Dopamine Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Adrenergic Agents
Adrenergic Uptake Inhibitors
Neurotransmitter Uptake Inhibitors
Dopamine Uptake Inhibitors
Narcotic Antagonists
Sensory System Agents

ClinicalTrials.gov processed this record on May 21, 2013