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Suboxone: (Buprenorphine/Naloxone) Comparison of Two Taper Schedules - 1 - Article


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Naloxone Injection

Narcan


Clinical Trial: Suboxone: (Buprenorphine/Naloxone) Comparison of Two Taper Schedules - 1

This study is currently recruiting patients.

Sponsors and Collaborators: National Institute on Drug Abuse (NIDA)
University of California, Los Angeles
Information provided by: National Institute on Drug Abuse (NIDA)

Purpose

The purpose of this protocol is to to compare the clinical utility of two dosage tapering regimens in Buprenorphine/Naloxone stabilized subjects for opiate detoxification.

Condition Treatment or Intervention Phase
Opioid-Related Disorders
 Drug: Buprenorphine
Phase III

MedlinePlus related topics:  Drug Abuse

Study Type: Interventional
Study Design: Treatment, Uncontrolled

Official Title: Suboxone: (Buprenorphine/Naloxone) Comparison of Two Taper Schedules

Further Study Details: 

Expected Total Enrollment:  509

Study start: January 2001

Eligibility

Ages Eligible for Study:  15 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Females are not pregnant or lactating
  • Subjects meet DSM-IV criteria for opiate dependence, are medically and psychiatrically stable, and do not have a current history of benzodiazepine dependence abuse, dependence, or treatment

Location and Contact Information

Jessica Fradis      (310)312-0500    jfradis@friendsresearch.org

Colorado
      Addiction Research & Treatment Services (ARTS), Denver,  Colorado,  80204,  United States; No longer recruiting

      Denver Health & Hospitals Authority, Denver,  Colorado,  80204,  United States; No longer recruiting

Connecticut
      Connecticut Counseling Centers, Waterbury,  Connecticut,  06705,  United States; Recruiting
Patricia Davis  203-755-8874 

      Hartford Dispensary, Hartford,  Connecticut,  06120,  United States; Recruiting
Mark Relyea  860-525-9376 

New York
      New York VA Medical Center, New York,  New York,  10010,  United States; Recruiting
Terry Leon  860-525-9376 

      LI Jewish Health System, Glen Oaks,  New York,  11004,  United States; Recruiting
Jessica Fradis  310-312-0500    jfradis@friendsresearch.org 

North Carolina
      Coastal Horizons Center, Inc., Wilmington,  North Carolina,  28412,  United States; Recruiting
Michael Yonkins  910-343-0145  Ext. 1065 

      South Light-Wakeview Clinic, Raleigh,  North Carolina,  27610,  United States; Recruiting
Denise Mcrae  919-832-4453  Ext. 212 

Oregon
      CODA, Portland,  Oregon,  97214,  United States; Recruiting
Sandy Kennard  503-239-8400 

Virginia
      Norfolk CSB, Norfolk,  Virginia,  23505,  United States; Recruiting
George Tucker  757-664-6683 

Washington
      Providence Behavioral Health Services, Everett,  Washington,  98201,  United States; No longer recruiting

Study chairs or principal investigators

Walter Ling, M.D.,  Principal Investigator,  University of California, Los Angeles   

More Information

Study ID Numbers:  NIDA-CTN-0003-1
Record last reviewed:  January 2005
Last Updated:  April 7, 2005
Record first received:  February 19, 2004
ClinicalTrials.gov Identifier:  NCT00078117
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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Page Updated: June 1, 2005
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