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Sponsors and Collaborators: |
National Institute on Drug Abuse (NIDA) University of Pennsylvania |
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Information provided by: | National Institute on Drug Abuse (NIDA) |
ClinicalTrials.gov Identifier: | NCT00000358 |
The purpose of this study is 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.
Condition | Intervention | Phase |
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Opioid-Related Disorders Substance-Related Disorders |
Drug: Lofexidine |
Phase I |
Study Type: | Interventional |
Study Design: | Treatment |
Official Title: | Safety Evaluation of Lofexidine for Treatment of Opioid Withdrawal |
Ages Eligible for Study: | 21 Years to 59 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Please contact site for information.
United States, Pennsylvania | |
University of Pennsylvania | |
Philadelphia, Pennsylvania, United States, 19104 6178 |
Principal Investigator: | Charles O'Brien, M.D., Ph.D. | PDVAMC Treatment Research Center |
Study ID Numbers: | NIDA-3-0012-7, Y01-3-0012-7 |
Study First Received: | September 20, 1999 |
Last Updated: | June 23, 2005 |
ClinicalTrials.gov Identifier: | NCT00000358 |
Health Authority: | United States: Federal Government |
Mental Disorders Substance-Related Disorders Disorders of Environmental Origin Lofexidine Opioid-Related Disorders |
Neurotransmitter Agents Disease Adrenergic alpha-Agonists Adrenergic Agents Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs Narcotic Antagonists Cardiovascular Agents |
Antihypertensive Agents Pharmacologic Actions Adrenergic Agonists Pathologic Processes Sensory System Agents Therapeutic Uses Peripheral Nervous System Agents Central Nervous System Agents |