- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Catalepsy.
Displaying page 1 of 1.
EudraCT Number: 2007-000800-34 | Sponsor Protocol Number: H8Y-MC-HBBI | Start Date*: 2007-08-14 | |||||||||||||||||||||||||||||||
Sponsor Name:Eli Lilly and Company Ltd. | |||||||||||||||||||||||||||||||||
Full Title: A Multi-center, Inpatient, Phase 2, Double-blind, Placebo-controlled Dose Ranging Study of LY2140023 in Patients with DSM-IV Schizophrenia. | |||||||||||||||||||||||||||||||||
Medical condition: Patients must have a diagnosis of Schizophrenia as defined in Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) (Disorganized, 295.10; Catatonic, 295.20; Paranoid, 295.... | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) PT (Completed) AT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000479-11 | Sponsor Protocol Number: 12396A | Start Date*: 2008-07-21 | ||||||||||||||||||||||||||
Sponsor Name:H. Lundbeck A/S | ||||||||||||||||||||||||||||
Full Title: A randomised, double-blind, parallel-group, active-controlled, flexible dose study exploring the efficacy and safety of 12 weeks treatment with Lu 31-130 in patients with schizophrenia | ||||||||||||||||||||||||||||
Medical condition: Lu 31-130 is under development by H. Lundbeck A/S as an antipsychotic in the treatment of schizophrenia | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: CZ (Completed) FR (Completed) ES (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022181-28 | Sponsor Protocol Number: 13639A | Start Date*: 2011-02-07 | ||||||||||||||||||||||||||
Sponsor Name:H. Lundbeck A/S | ||||||||||||||||||||||||||||
Full Title: A 6-month, randomised, double-blind, parallel-group, risperidone-controlled, fixed-dose study evaluating the safety and efficacy of zicronapine in patients with schizophrenia | ||||||||||||||||||||||||||||
Medical condition: Schizophrenia | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FI (Completed) EE (Completed) CZ (Completed) PL (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-009215-22 | Sponsor Protocol Number: BISCLOZ | Start Date*: 2009-03-26 | |||||||||||||||||||||||||||||||
Sponsor Name:Aalborg Psychiatric Hospital, Centre for Skizophrenia | |||||||||||||||||||||||||||||||||
Full Title: “Treating clozapine-induced sinustachycardia (BISCLOZ).” | |||||||||||||||||||||||||||||||||
Medical condition: Clozapine induced sinuatachycardia treated with bisoprolol. | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024488-42 | Sponsor Protocol Number: 2010-024488-42-PACS | Start Date*: 2011-01-31 | |||||||||||||||||||||||||||||||
Sponsor Name:Aalborg University Hospital, Aalborg Psychiatric Hospital, Centre for Psychosisresearch | |||||||||||||||||||||||||||||||||
Full Title: Pregabalin for anxiety comorbidity in patients with schizophrenia (PACS) - A Double-blinded Randomized Placebo Controlled Trial | |||||||||||||||||||||||||||||||||
Medical condition: anxiety-comorbidity to schizophrenia | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-008366-13 | Sponsor Protocol Number: 3.0edition | Start Date*: 2009-03-17 | |||||||||||||||||||||||||||||||
Sponsor Name:Unit for Psychiatric Research | |||||||||||||||||||||||||||||||||
Full Title: Comparison of the effects of Sertindole and Olanzapine on Cognition | |||||||||||||||||||||||||||||||||
Medical condition: Cognitive deficits in patients with schizophrenia | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) SE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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