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Bluelighter
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Summary:
http://www.clinicaltrials.gov/ct/show/NCT00476242
Inclusion Criteria:
Adult, aged 18-60.
Meets DSM-IV criteria for current opiate dependence disorder of at least six months duration, supported by a positive urine for opiates and a positive naloxone challenge test if the diagnosis is unclear.
Able to give informed consent.
Exclusion Criteria:
Pregnancy, lactation, or failure in a sexually active woman to use adequate contraceptive methods.
Active medical illness which might make participation hazardous, such as untreated hypertension, acute hepatitis with SGOT or SGPT levels >2 times normal, unstable diabetes, chronic organic mental disorder (e.g., AIDS dementia).
Active psychiatric disorder which might interfere with participation or make participation hazardous, including DSM-IV schizophrenia, bipolar disorder with mania or psychosis, and depressive disorder with suicide risk or 1 or more suicide attempts within the past year.
History of allergic reaction to buprenorphine, naloxone, memantine, naltrexone, clonidine, or clonazepam.
Currently prescribed or regularly taking opiates for chronic pain or medical illness.
Current participation in another intensive psychotherapy or substance abuse treatment program or currently prescribed psychotropic medications.
Current participation in a methadone maintenance treatment program and/or regular use of illicit methadone (>30 mg per week).
History of accidental drug overdose in the last three years or any other significant history of overdose following detoxification defined as an episode of opioid-induced unconsciousness or incapacitation, whether or not medical treatment was sought or received.
Started June 2005; currently in progress and accepting new participants.
Contact
Please refer to this study by ClinicalTrials.gov identifier NCT00476242
Kovi Yaacov, BA 212- 923-3031
United States, New York
STARS, New York, New York, 10032, United States; Recruiting
Kovi Elkus, BA 212-923-3031
Adam Bisaga, MD, Principal Investigator
(Please do not PM me in regards to this, I am not affiliated with this research)
Free treatment for heroin or opiate abuse. Research study involves inpatient detox and outpatient care.
The number of new heroin users and problems associated with heroin use has increased steadily over the past several years. While methadone maintenance remains the most effective treatment for opioid dependence, it has several limitations and is controversial.
Naltrexone maintenance is an alternate treatment for opiate dependence that is promising, but currently has limited usefulness due to poor patient compliance and low patient acceptability. There is strong support from animal research that another class of drugs, NMDA-R antagonists, may also be an effective treatment for opiate dependence. In laboratory animals, NMDA-R antagonists have inhibited behaviors associated with relapse, reduced opiate self-administration, and helped with withdrawal symptoms. In humans, NMDA-R antagonists have reduced signs and symptoms associated with opiate withdrawal and reduced heroin craving. The primary aim of this study is to determine the efficacy of memantine as an adjunct to naltrexone maintenance in detoxified heroin-dependent individuals.
Prospective participants will undergo a screening process at the clinic to determine eligibility. After screening, eligible patients will complete an 8-day inpatient detoxification, followed by a 12-week outpatient phase. During the outpatient phase, patients will be assigned to one of three medication groups: 1) Naltrexone + Placebo; 2) Naltrexone + Memantine 30 mg twice daily; 3) Naltrexone + Memantine 60 mg twice daily. The outpatient treatment will also consist of 3 weekly visits to the clinic in which patients will receive counseling to help maintain abstinence and improve compliance with study medication. In addition to providing treatment referrals, follow up assessments will be completed one, two, and three months after the completion of treatment.
http://www.clinicaltrials.gov/ct/show/NCT00476242
Inclusion Criteria:
Adult, aged 18-60.
Meets DSM-IV criteria for current opiate dependence disorder of at least six months duration, supported by a positive urine for opiates and a positive naloxone challenge test if the diagnosis is unclear.
Able to give informed consent.
Exclusion Criteria:
Pregnancy, lactation, or failure in a sexually active woman to use adequate contraceptive methods.
Active medical illness which might make participation hazardous, such as untreated hypertension, acute hepatitis with SGOT or SGPT levels >2 times normal, unstable diabetes, chronic organic mental disorder (e.g., AIDS dementia).
Active psychiatric disorder which might interfere with participation or make participation hazardous, including DSM-IV schizophrenia, bipolar disorder with mania or psychosis, and depressive disorder with suicide risk or 1 or more suicide attempts within the past year.
History of allergic reaction to buprenorphine, naloxone, memantine, naltrexone, clonidine, or clonazepam.
Currently prescribed or regularly taking opiates for chronic pain or medical illness.
Current participation in another intensive psychotherapy or substance abuse treatment program or currently prescribed psychotropic medications.
Current participation in a methadone maintenance treatment program and/or regular use of illicit methadone (>30 mg per week).
History of accidental drug overdose in the last three years or any other significant history of overdose following detoxification defined as an episode of opioid-induced unconsciousness or incapacitation, whether or not medical treatment was sought or received.
Started June 2005; currently in progress and accepting new participants.
Contact
Please refer to this study by ClinicalTrials.gov identifier NCT00476242
Kovi Yaacov, BA 212- 923-3031
United States, New York
STARS, New York, New York, 10032, United States; Recruiting
Kovi Elkus, BA 212-923-3031
Adam Bisaga, MD, Principal Investigator
(Please do not PM me in regards to this, I am not affiliated with this research)
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