Naloxone Injection |
Narcan |
Clinical Trial: Suboxone: (Buprenorphine/Naloxone) Comparison of Two Taper Schedules - 1
This study is currently recruiting patients.
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
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
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
Hartford Dispensary, Hartford, Connecticut, 06120, United States; Recruiting
New York
New York VA Medical Center, New York, New York, 10010, United States; Recruiting
LI Jewish Health System, Glen Oaks, New York, 11004, United States; Recruiting
North Carolina
Coastal Horizons Center, Inc., Wilmington, North Carolina, 28412, United States; Recruiting
South Light-Wakeview Clinic, Raleigh, North Carolina, 27610, United States; Recruiting
Oregon
CODA, Portland, Oregon, 97214, United States; Recruiting
Virginia
Norfolk CSB, Norfolk, Virginia, 23505, United States; Recruiting
Washington
Providence Behavioral Health Services, Everett, Washington, 98201, United States; No longer recruiting
Walter Ling, M.D., Principal Investigator, University of California, Los Angeles
More Information
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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