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Safety Evaluation of Lofexidine for Treatment of Opioid Withdrawal - 7



Safety Evaluation of Lofexidine for Treatment of Opioid Withdrawal - 7

For Condition: Opioid-Related Disorders,Substance-Related Disorders
Status: Completed
Sponsor(s): National Institute on Drug Abuse (NIDA) , University of Pennsylvania
Synopsis: To determine the safety of lofexidine in the treatment of opiate withdrawal. Preliminary data will also be obtained to assess the ability of lofexidine to alleviate opiate withdrawal signs and symptoms. (high dose study).
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Uncontrolled
Minimum Age/Maximum Age: 21 Years/59 Years
Genders: Both
Protocol Entry Criteria: Please contact site for information.
Total Enrollment: 0

Location and Contact Information:

Overall Study Official:
CharlesO'Brien,  Principal Investigator,  PDVAMC Treatment Research Center

University of Pennsylvania
Philadelphia,  Pennsylvania,  19104 6178
United States
 


Additional Information:
Study ID Numbers:
  NIDA-3-0012-7; 
Study Start Date: 
Record last reviewed: December 2002
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000358

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5. Methamphetamine Abuse Pharmacology in Patients with AIDS - 1

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