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| Sponsors and Collaborators: |
National Institute on Drug Abuse (NIDA) Yale University |
|---|---|
| Information provided by: | National Institute on Drug Abuse (NIDA) |
| ClinicalTrials.gov Identifier: | NCT00000192 |
Purpose
The purpose of this study is to evaluate the effects of lamotrigine on naloxone-precipitated opiate withdrawal.
| Condition | Intervention | Phase |
|---|---|---|
|
Opioid-Related Disorders |
Drug: Lamotrigine |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Double-Blind, Placebo Control |
| Official Title: | Neurobiology of Opioid Dependence: 1 |
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Please contact site for information.
Contacts and Locations| United States, Connecticut | |
| VA Connecticut Healthcare System | |
| New Haven, Connecticut, United States, 06519 | |
| Principal Investigator: | Marc I Rosen, M.D. | VA Connecticut Healthcare System |
More Information
| Study ID Numbers: | NIDA-00191-1, K20-00191-1 |
| Study First Received: | September 20, 1999 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00000192 History of Changes |
| Health Authority: | United States: Federal Government |
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Calcium, Dietary Mental Disorders Lamotrigine Substance-Related Disorders Calcium Channel Blockers |
Disorders of Environmental Origin Cardiovascular Agents Opioid-Related Disorders Anticonvulsants |
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Molecular Mechanisms of Pharmacological Action Disorders of Environmental Origin Calcium Channel Blockers Cardiovascular Agents Opioid-Related Disorders Pharmacologic Actions Membrane Transport Modulators |
Mental Disorders Therapeutic Uses Substance-Related Disorders Lamotrigine Central Nervous System Agents Anticonvulsants |