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| Sponsor: | National Institute on Drug Abuse (NIDA) |
|---|---|
| Collaborator: |
University of Pennsylvania |
| Information provided by: | National Institute on Drug Abuse (NIDA) |
| ClinicalTrials.gov Identifier: | NCT00000358 |
Purpose
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 |
|---|---|---|
|
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 |
Eligibility| Ages Eligible for Study: | 21 Years to 59 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Please contact site for information.
Contacts and Locations| 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 |
More Information
| 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 History of Changes |
| Health Authority: | United States: Federal Government |
|
Neurotransmitter Agents Disease Adrenergic alpha-Agonists Molecular Mechanisms of Pharmacological Action Adrenergic Agents Narcotic Antagonists Physiological Effects of Drugs Disorders of Environmental Origin Cardiovascular Agents Opioid-Related Disorders Lofexidine |
Antihypertensive Agents Pharmacologic Actions Adrenergic Agonists Pathologic Processes Sensory System Agents Mental Disorders Therapeutic Uses Substance-Related Disorders Peripheral Nervous System Agents Central Nervous System Agents |