Schizophrenia Clinical Trial
Official title:
Solian Solution to Treat Schizophrenic Patients During an Acute Episode
| Verified date | April 2008 |
| Source | Sanofi |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Belgium: Federal Agency for Medicines and Health Products, FAMHP |
| Study type | Interventional |
During this study the efficacy and safety profile will be evaluated of the use of
amisulpride in the form of a solution in schizophrenic patients with an acute episode.
The main purpose of the study is to observe the anti-psychotic effect of amisulpride as a
solution during the first days of an acute episode of schizophrenia.
| Status | Completed |
| Enrollment | 300 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years to 65 Years |
| Eligibility |
Inclusion Criteria: - schizophrenic in-patients with an acute episode - aged between 18 and 65 years - written informed consent Exclusion Criteria: - pregnancy and breast-feeding - breast cancer, prolactinoma, pheochromocytoma - hypersensitivity to amisulpride or one of the other excipients - contra-indications when using amisulpride as per the SmPC |
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Belgium | Sanofi-aventis | Diegem |
| Lead Sponsor | Collaborator |
|---|---|
| Sanofi |
Belgium,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | *analyze the antipsychotic efficacy of amisulpride solution in the first days of an acute schizophrenic episode. | |||
| Secondary | *analyse the safety profile of amisulpride solution in treatment of schizophrenics with an an acute episode. |
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