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Completed

NCT Number: NCT01100853

Extended Release Naltrexone for Treating Amphetamine Dependence in Iceland

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

SAA National Center of Addiction Medicine, Vogur Hospital

Storhofda 45, Reykjavík, 112, Iceland

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

VIVITROL injection and VIVITROL Placebo Injection , 24 weeks

Drug

Efficacy of 24 week course of VIVITROL with counseling as compared to 24 week course of VIVITROL placebo with counseling (monthly injections)

Primary outcomes

  1. Number Negative Urines (Proportion Negative Urines)

    Time frame: 24 Weeks

  2. Number Negative Urines (Proportion Negative Urines) Amphetamine

    Time frame: 24 weeks

Secondary outcomes

  1. Amphetamine Craving Scale

    Time frame: 24 weeks

    The Amphetamine Craving Scale is a visual analogue scale, which is scored by indicating the level of craving on a 100 mm line, where 0 is no craving at all and 100 is the highest level of craving experienced. Scores are derived from measuring their placement on the line, yielding scores from 0 to 100.

  2. Beck Depression Inventory

    Time frame: 24 weeks

    The Beck Depression Inventory is a self-administered questionnaire that assess the severity of depressive symtpoms. It consists of 21 items about how the subject has been feeling in the last week, and each item has a set of at least four possible answer choices, ranging in intensity, yielding scores from 0-3, with a total possible score of 63. Higher scores indicate more severe depressive symptoms.

  3. Risk Assessment Battery

    Time frame: 24 weeks

    The Risk Assessment Battery is a 41 item self-report questionnaire that assess risk behaviors related to HIV infection over the past 6 months. The measure yields a Drug risk score ranging from 0-22 and a Sex risk score ranging from 0-18, with higher scores indicating more risk; these scores are added to yield a Total RAB score ranging from 0-40. This total scores is then divided by 40 to yield a RAB Scale Score from 0-1.

  4. Prior Admissions to Vogur Hospital

    Time frame: Baseline

    Number of prior admissions due to substance dependence. The term "prior admissions" refers to admissions before enrollment, thus Baseline is the appropriate Time Frame.

Sponsors and collaborators

Lead sponsor

University of Pennsylvania

Other

Collaborators

  • National Institute on Drug Abuse (NIDA)
  • Society of Alcoholism and other Addictions

Registry information

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
Apr 9, 2010
Registry last updated
Mar 6, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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