- Trials with a EudraCT protocol (45)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
45 result(s) found for: Risperdal.
Displaying page 1 of 3.
| EudraCT Number: 2005-002304-41 | Sponsor Protocol Number: RIS-SCH-4045 | Start Date*: 2005-09-23 |
| Sponsor Name:Janssen-Cilag EMEA Medical Affairs | ||
| Full Title: Early versus late initiation of treatment with Risperdal Consta in subjects with schizophrenia or schizoaffective disorder after an acute episode | ||
| Medical condition: Schizophrenia or schizoaffective disorder. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) DK (Completed) FI (Completed) GB (Completed) SI (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-004482-15 | Sponsor Protocol Number: NRA 1280013 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Universitätsklinikum Aachen, Klinik f. Psychiatrie und Psychotherapie | ||
| Full Title: Hirnaktivierung während Gedächtnisaufgaben bei Patienten mit Schizophrenie unter Behandlung von Ziprasidon oder Risperidon. Eine FMRT-Untersuchung. | ||
| Medical condition: Patienten mit DSM-IVTR diagnostizierter Schizophrenie | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-003781-14 | Sponsor Protocol Number: RISBIM3003 | Start Date*: 2004-12-02 |
| Sponsor Name:Johnson & Johnson Pharmaceutical Research and Development | ||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Explore the Efficacy and Safety of Risperidone Long-Acting Intramuscular Injectable in the Prevention of Mood Episodes in Bipolar I Disorder,... | ||
| Medical condition: BIPOLAR MANIA | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) SK (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-000870-29 | Sponsor Protocol Number: RISSCH3001 | Start Date*: 2004-11-04 |
| Sponsor Name:Janssen-Cilag Medical Affairs EMEA | ||
| Full Title: CONSTATRE Risperdal Consta Trial of Relapse Prevention and Effectiveness | ||
| Medical condition: SCHIZOPHRENIA, SCHIZOAFFECTIVE DISORDER | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: HU (Completed) ES (Completed) AT (Completed) SE (Completed) CZ (Completed) LV (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-002694-22 | Sponsor Protocol Number: R092670PSY3002 | Start Date*: 2005-02-07 |
| Sponsor Name:Janssen-Cilag International N.V | ||
| Full Title: A Randomized, Double-Blind, Parallel Group Non-inferiority Study of Flexibly Dosed Paliperidone Palmitate(25, 50, 75, 100 mg eq) Administered Every 4 weeks and Flexibly Dosed Risperdal Consta (25, ... | ||
| Medical condition: schizophrenia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) AT (Completed) SE (Completed) CZ (Completed) DK (Completed) EE (Completed) ES (Completed) LT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-004857-27 | Sponsor Protocol Number: F20REWARDLU | Start Date*: 2008-01-02 |
| Sponsor Name:Department of Psychiatry and Psychotherapy, Ludwig-Maximilians-University Munich | ||
| Full Title: Ventral striatal function in patients with schizophrenia before and under medication with atypical antipsychotics: a comparison of sertindole and risperidone | ||
| Medical condition: schizophrenic patients (F20.0, F20.1, F20.2, F20.3, F20.5, F20.6, F20.8, F20.9) and healthy controls | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-004383-23 | Sponsor Protocol Number: RISSCH4055 | Start Date*: 2005-11-24 |
| Sponsor Name:Janssen Cilag Ltd | ||
| Full Title: Pragmatic randomized trial of Risperdal Consta versus oral atypical antipsychotics in poorly adherent subjects with schizophrenia ina routine care setting. Protocol RISSCH4055; Phase IV (risperid... | ||
| Medical condition: Schizophrenia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) IE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-004621-25 | Sponsor Protocol Number: RIS-SCH-4043 | Start Date*: 2006-01-30 | |||||||||||
| Sponsor Name:Janssen-Cilag Medical Affairs EMEA | |||||||||||||
| Full Title: Is premorbid functioning a predictor of outcome in patients with early onset psychosis treated with Risperdal Consta? | |||||||||||||
| Medical condition: Schizophrenia, schizoaffective disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: LT (Completed) NL (Completed) BE (Completed) IT (Completed) PT (Completed) GR (Completed) IE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001490-15 | Sponsor Protocol Number: RIS-BMN-3001 | Start Date*: 2007-04-23 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V | |||||||||||||
| Full Title: A randomized, double-blind, placebo- and active-controlled, parallel-group study to evaluate the efficacy and safety of risperidone long-acting injectable for the prevention of mood episodes in the... | |||||||||||||
| Medical condition: Subjects with a diagnosos of bipolar I disorder who are currently experiencing a manic or mixed episode (YMRS>20 and CGI-S>/= 4 [moderate]) or who are between mood episodes (non-acute; YMRS<12 and ... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012003-26 | Sponsor Protocol Number: RIS-NAP-4022 | Start Date*: 2010-04-13 | |||||||||||||||||||||
| Sponsor Name:Janssen-Cilag International, NV | |||||||||||||||||||||||
| Full Title: Evaluation of Growth, Sexual Maturation, and Prolactin-Related Adverse Events in the Pediatric Population Exposed to Atypical Antipsychotic Drugs | |||||||||||||||||||||||
| Medical condition: Long-term safety data in children and adolescents will be collected from a population of patients with a diagnosis of schizophrenia, bipolar mania, autistic disorder or conduct and other disruptive... | |||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Prematurely Ended) BE (Prematurely Ended) GR (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2006-004891-10 | Sponsor Protocol Number: Vocational Rehabilitation | Start Date*: 2007-04-17 | |||||||||||
| Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
| Full Title: Future strategies for vocational rehabilitation schizophrenia | |||||||||||||
| Medical condition: The social implications and long-term consequences of mental disorders regarding sick days at work, unemployment rates and early retirement are considerable. This trial is being conducted to unders... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004034-32 | Sponsor Protocol Number: 17-216 | Start Date*: 2006-09-20 |
| Sponsor Name:Medizinische Universität Graz | ||
| Full Title: Zur Frage des neuroleptikainduzierten metabolischen Syndroms. Studie 1: Fettverteilung und spezifische hormonelle Parameter. Eine prospektive Vergleichsstudie zwischen 5 atypischen Neuroleptika | ||
| Medical condition: Einschlusskriterien: - Schizophrenie, schizoaffektive Störung oder akut polymorph psychotische Störung - Alter: zwischen 18 und 70 Jahren - Vorliegen einer schriftlichen Einverständniserklärung zu... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-004740-79 | Sponsor Protocol Number: D1443L00039 | Start Date*: 2008-06-10 |
| Sponsor Name:AstraZeneca GmbH | ||
| Full Title: A One-Year Randomized, Prospective, Parallel, Open Comparison of Subjective Well-being in Schizophrenic Out-patients Treated with Quetiapine XR (SEROQUEL Prolong®) or Oral Risperidone at Flexible D... | ||
| Medical condition: Schizophrenia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) FI (Completed) BE (Completed) PT (Completed) IT (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-003340-11 | Sponsor Protocol Number: R076477SCH4026 | Start Date*: 2008-11-03 | |||||||||||
| Sponsor Name:JANSSEN-CILAG GmbH | |||||||||||||
| Full Title: The “therapeutic window” of the "atypical” antipsychotic paliperidone ER - A Positron Emission Tomography study with [18F]fallypride as the radiotracer | |||||||||||||
| Medical condition: subchronic schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-005010-22 | Sponsor Protocol Number: LY03004/CT-EUR-101 | Start Date*: 2019-04-26 | |||||||||||
| Sponsor Name:Nanjing Luye Pharmaceutical Co., Ltd. | |||||||||||||
| Full Title: A Randomized, Open-Label, Cross-over Study to Assess the Relative Bioavailability of LY03004 and EU Risperdal® Consta® at 50 mg Following Multiple Intramuscular Injections in Stable Patients with S... | |||||||||||||
| Medical condition: schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004246-32 | Sponsor Protocol Number: D1443L00031 | Start Date*: 2007-12-05 | |||||||||||
| Sponsor Name:ASTRAZENECA | |||||||||||||
| Full Title: Comparison of Quetiapine Extended-Release (Seroquel XR ) and Risperidone in the treatment of depressive symptoms, in schizophrenic or schizoaffective patients: A randomized, open label, flexible-d... | |||||||||||||
| Medical condition: Patient with schizophrenia or schizoaffective disorder with depressive symptoms | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005772-13 | Sponsor Protocol Number: AMISU_L_01008 | Start Date*: 2008-01-28 |
| Sponsor Name:sanofi-aventis Zrt. | ||
| Full Title: Comparative efficacy of amisulpride vs. risperidone on cognitive functions in patients with chronic schizophrenia. | ||
| Medical condition: measure of overall cognitive functioning in chronic schizophrenia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: HU (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-002979-33 | Sponsor Protocol Number: RIS-USA-234 | Start Date*: 2006-01-19 |
| Sponsor Name:Janssen-Cilag International N.V. | ||
| Full Title: Estudio de la eficacia y seguridad de risperidona en el tratamiento de adolescentes con esquizofrenia: Estudio abierto de seis meses. | ||
| Medical condition: SCHIZOPHRENIA/ Adolescents | ||
| Disease: | ||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-011594-33 | Sponsor Protocol Number: SMRI-07TGF-1152 | Start Date*: 2009-11-02 | |||||||||||
| Sponsor Name:LWL University Hospital Bochum, Ruhr-University Bochum | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled study of tetrabenazine as adjunctive therapy to risperidone in first-episode schizophrenia | |||||||||||||
| Medical condition: Schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-005485-36 | Sponsor Protocol Number: RGH-188-005 | Start Date*: 2013-04-17 | |||||||||||
| Sponsor Name:Gedeon Richter Plc | |||||||||||||
| Full Title: A kariprazin hatásosságának, biztonságosságának és tolerálhatóságának randomizált, kettős vak, párhuzamos csoportos vizsgálata túlnyomórészt negatív tünetes skizofrén betegeknél | |||||||||||||
| Medical condition: Patients with Predominant Negative Symptoms of Schizophrenia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) ES (Completed) PL (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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