- Trials with a EudraCT protocol (28)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28 result(s) found for: Schizoaffective Disorder AND Placebo.
Displaying page 1 of 2.
| EudraCT Number: 2006-005734-20 | Sponsor Protocol Number: R076477-SCA-3002 | Start Date*: 2008-04-24 | |||||||||||
| Sponsor Name:Janssen L.P. | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy and Safety of Flexible Dose Paliperidone ER in the Treatment of Subjects with Schizoaffective Disorder | |||||||||||||
| Medical condition: Schizoaffective disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004494-81 | Sponsor Protocol Number: PNB02-C201 | Start Date*: 2012-03-29 | ||||||||||||||||
| Sponsor Name:Pharmaneuroboost N.V. | ||||||||||||||||||
| Full Title: Proof-of-Concept Study of Pipamperone 15mg added to Stable Treatment with Risperidone or Paliperidone in Chronic Schizophrenic and Schizoaffective Patients with Residual Symptoms: a phase I/IIa, r... | ||||||||||||||||||
| Medical condition: Schizophrenia or Schizoaffective disorder according to the Diagnostic and Statistical Manual of Mental Disorders (DSM)-IV-R criteria. | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-000757-36 | Sponsor Protocol Number: ASA-CRP-01 | Start Date*: 2014-10-07 | ||||||||||||||||
| Sponsor Name:Clinirx Tangent Research | ||||||||||||||||||
| Full Title: A randomized trial administering aspirin vs. placebo as add-on to antipsychotics in patients with schizophrenia or schizoaffective disorder with high CRP levels | ||||||||||||||||||
| Medical condition: schizophrenia and schizoaffective disorder. | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: RO (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-017271-17 | Sponsor Protocol Number: R092670-SCA-3004 | Start Date*: 2010-10-29 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of Paliperidone Palmitate Evaluating Time to Relapse in Subjects With Schizoaffective Disorder | |||||||||||||
| Medical condition: Schizoaffective Disorder | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004752-16 | Sponsor Protocol Number: BP40283 | Start Date*: 2021-07-30 | ||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
| Full Title: PHASE 2, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO ASSESS THE EFFECTS OF RO6889450 (RALMITARONT) IN PATIENTS WITH SCHIZOPHRENIA OR SCHIZOAFFECTIVE DISORDER AND NEGATIVE SYMPTOMS | ||||||||||||||||||
| Medical condition: Schizophrenia or schizoaffective disorder | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Prematurely Ended) PL (Prematurely Ended) BG (Prematurely Ended) HR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-004483-11 | Sponsor Protocol Number: 80-83600-98-40120 | Start Date*: 2016-07-08 | |||||||||||||||||||||
| Sponsor Name:University Medical Center Utrecht | |||||||||||||||||||||||
| Full Title: Raloxifene Augmentation in Patients with a Schizophrenia spectrum Disorder to reduce symptoms and improve cognition | |||||||||||||||||||||||
| Medical condition: schizophrenia, schizoaffective, schizophreniform disorder or psychosis not otherwhise specified (DSM-IV 295.*) | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Completed) BE (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2010-024065-46 | Sponsor Protocol Number: 2010-379 | Start Date*: 2011-05-03 | |||||||||||||||||||||
| Sponsor Name:Lone Baandrup | |||||||||||||||||||||||
| Full Title: Melatonin vs. placebo til nedtrapning af benzodiazepiner hos patienter med skizofreni: et randomiseret klinisk forsøg (SMART) | |||||||||||||||||||||||
| Medical condition: Patienter med kronisk skizofreni og i længerevarende behandling med en kombination af antipsykotika og benzodiazepiner. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2013-000415-25 | Sponsor Protocol Number: NAS-S-01 | Start Date*: 2013-11-07 | ||||||||||||||||
| Sponsor Name:Clinirx Tangent Research | ||||||||||||||||||
| Full Title: A randomized, double-blind, placebo controlled study to evaluate the efficacy and safety of Naproxen, Simvastatin and their combination, compared to placebo as add-on to anti-psychotics in the trea... | ||||||||||||||||||
| Medical condition: schizophrenia and schizoaffective disorder. | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: RO (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2017-004064-35 | Sponsor Protocol Number: | Start Date*: 2018-04-17 |
| Sponsor Name:Southern Health NHS Foundation Trust | ||
| Full Title: Liraglutide and the management of overweight and obesity in people with schizophrenia: a pilot study | ||
| Medical condition: Schizophrenia, schizoaffective disorder or first episode psychosis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-004489-16 | Sponsor Protocol Number: V3_KET_NEG_SYMPT_SCZ | Start Date*: 2021-11-03 |
| Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Psychiatrie und Psychotherapie | ||
| Full Title: Ketamine for the treatment of depressive and negative symptoms in patients with schizophrenia: a randomized controlled cross-over pilot study. | ||
| Medical condition: Negative and depressive symptoms of schizophrenia according to DSM-5 | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-000520-14 | Sponsor Protocol Number: NL46653 | Start Date*: 2014-07-31 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: Prednisolone addition for atients with recent onset psychotic disorder: the role of immune-modulating strategies in the treatment of psychosis. | ||
| Medical condition: Schizophrenia, schizophreniphorm disorder, schizoaffective disorder, psychosis NOS. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-000163-32 | Sponsor Protocol Number: NorPEPS | Start Date*: 2017-06-29 |
| Sponsor Name:Helse-Bergen HF | ||
| Full Title: The Norwegian Prednisolone in Early Psychosis Study - NorPEPS The role of immune-modulating strategies in the treatment of psychosis | ||
| Medical condition: Schizophrenia, schizophreniphorm disorder, schizoaffective disorder, psychosis NOS. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-006048-42 | Sponsor Protocol Number: P04628 | Start Date*: 2006-09-05 | |||||||||||
| Sponsor Name:Schering-Plough Research Institute | |||||||||||||
| Full Title: A Phase 2a, Multiple-Dose, Placebo Controlled, Randomized, Two Way Crossover Study to Assess the Efficacy of SCH 420814 in Reducing Anti-Psychotic-Induced Extra-Pyramidal Symptoms Among Subjects Wi... | |||||||||||||
| Medical condition: Patients with schizophrenia and schizoaffective disorders experiencing anti-psychotic-induced extra-pyramidal symptoms. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003008-53 | Sponsor Protocol Number: 80836009820016 | Start Date*: 2014-12-10 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: Clonidine Augmentation Therapy in Schizophrenia | ||
| Medical condition: Schizophrenia, schizophreniform disorder, schizoaffective disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-000834-36 | Sponsor Protocol Number: 43806 | Start Date*: 2013-09-26 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: Simvastatin addition to improve symptoms, cognition and metabolic syndrome in patients with recent-onset schizophrenia. | ||
| Medical condition: Schizophrenia, schizoaffective or schizophreniform disorder (DSM-IV 295.*) or psychosis NOS (not otherwise specified) (298.9) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-000053-27 | Sponsor Protocol Number: MELIA | Start Date*: 2020-07-09 |
| Sponsor Name:UMC Utrecht | ||
| Full Title: The MEtformin-LIfestyle in Antipsychotic users trial (MELIA): optimizing the use of metformin in the management of antipsychotic-induced weight gain. | ||
| Medical condition: Antipsychotic-induced weight gain (AiWG) | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-023983-42 | Sponsor Protocol Number: RAL-S-01 | Start Date*: 2011-09-13 |
| Sponsor Name: The Stanley Medical Research Institute | ||
| Full Title: A randomized trial administering Raloxifene vs. Placebo as add-on to antipsychotics in post menopausal patients with schizophrenia or schizoaffecive disorder | ||
| Medical condition: schizophrenia or schizoaffecive disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: RO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001337-40 | Sponsor Protocol Number: BXCL501-105 | Start Date*: 2021-10-05 | |||||||||||||||||||||
| Sponsor Name:BioXcel Therapeutics, Inc. | |||||||||||||||||||||||
| Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO DETERMINE EFFICACY AND SAFETY OF BXCL501 IN AGITATION ASSOCIATED WITH PEDIATRIC SCHIZOPHRENIA AND BIPOLAR DISORDER | |||||||||||||||||||||||
| Medical condition: Subject that meets DSM-5 criteria for schizophrenia, schizoaffective, or schizophreniform disorder, or other specified/unspecified schizophrenia spectrum and/or other psychotic disorders OR Subjec... | |||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Restarted) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2016-003529-41 | Sponsor Protocol Number: ABR58805 | Start Date*: 2017-02-22 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: CANGLIA: Endocannabinoid control of microglia activation as a new therapeutic target in the treatment of schizophrenia | ||
| Medical condition: Schizophrenia patients | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-023982-23 | Sponsor Protocol Number: MAP-S-01 | Start Date*: 2011-08-22 |
| Sponsor Name:The Stanley Medical Research Institute | ||
| Full Title: A randomized trial administering Minocycline, Acetylsalicylic acid or Pramipexole vs Placebo as add-on to antipsychotics in patients with schizophrenia or schizoaffecive disorder | ||
| Medical condition: schizophrenia or schizoaffecive disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: RO (Completed) | ||
| Trial results: (No results available) | ||
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