Opioid-Related Disorders Clinical Trial
Official title:
Neurobiology of Opioid Dependence: 1
| Verified date | August 2015 |
| Source | Yale University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Federal Government |
| Study type | Interventional |
The purpose of this study is to evaluate the effects of lamotrigine on naloxone-precipitated opiate withdrawal.
| Status | Withdrawn |
| Enrollment | 0 |
| Est. completion date | January 1998 |
| Est. primary completion date | January 1998 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | N/A and older |
| Eligibility | Please contact site for information. |
Masking: Double-Blind, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United States | VA Connecticut Healthcare System | New Haven | Connecticut |
| Lead Sponsor | Collaborator |
|---|---|
| Yale University | National Institute on Drug Abuse (NIDA) |
United States,
Rosen MI, Pearsall HR, Kosten TR. The effect of lamotrigine on naloxone-precipitated opiate withdrawal. Drug Alcohol Depend. 1998 Oct 1;52(2):173-6. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Behavioral, subjective, measures of naloxone-precipitated opiate withdrawal | |||
| Primary | Phsyiological, neuroendocrine measures of naloxone-precipitated opiate withdrawal |
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