- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
22 result(s) found for: Yale-Brown Obsessive Compulsive Scale.
Displaying page 1 of 2.
EudraCT Number: 2011-002819-28 | Sponsor Protocol Number: OCDDCS001 | Start Date*: 2012-04-12 | |||||||||||
Sponsor Name:Stockholms Läns Landsting | |||||||||||||
Full Title: Internet-based cognitive behavior therapy in combination with D-Cycloserine for Obsessive Compulsive Disorder: A double blinded randomized controlled trial | |||||||||||||
Medical condition: Obsessive Compulsive disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016713-20 | Sponsor Protocol Number: CL2-20098-072 | Start Date*: 2010-04-13 | |||||||||||
Sponsor Name:Laboratorios Servier S.L. | |||||||||||||
Full Title: Eficacia de agomelatina 25mg/día (con posibilidad de incremento a 50mg/día tras 8 semanas de tratamiento) por vía oral durante 16 semanas en pacientes con Trastorno Obsesivo Compulsivo // Efficacy... | |||||||||||||
Medical condition: Trastorno Obsesivo Compulsivo // Obsessive-compulsive disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016751-22 | Sponsor Protocol Number: ABR30311 | Start Date*: 2010-04-01 | |||||||||||
Sponsor Name:AMC, divisie Psychiatrie | |||||||||||||
Full Title: A double blind, placebo controlled study of memantine in patients with obsessive-compulsive disorder. | |||||||||||||
Medical condition: Obsessive-compulsive disorder (OCD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006947-38 | Sponsor Protocol Number: RAA2008-014 | Start Date*: 2009-01-15 | |||||||||||
Sponsor Name:King's College London (Institute of Pyschiatry) | |||||||||||||
Full Title: A randomised double-blind placebo-controlled pilot study of D-cycloserine-augmented exposure therapy in adolescents with obsessive-compulsive disorder | |||||||||||||
Medical condition: Obsessive-compulsive disorder (OCD) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003228-34 | Sponsor Protocol Number: OCMDKET | Start Date*: 2022-04-25 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Ketamine therapy and its effects on stress on neuropsychological function under stress in obsessive-compulsive disorder | ||
Medical condition: Obsessive-compulsive disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011115-20 | Sponsor Protocol Number: NordLOTS protocol step 3 1.1 | Start Date*: 2009-08-14 | ||||||||||||||||
Sponsor Name:The Centre for Child and Adolescent Mental Health, Eastern and Southern Norway (R.BUP) | ||||||||||||||||||
Full Title: Nordic Longterm OCD treatment Study: A Nordic Multicenter treatment study evaluating a stepped care model based on the "Expert Clinical Guidelines". The study is performed with no sponsor from phar... | ||||||||||||||||||
Medical condition: Obsessive Compulsive Disorder | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Ongoing) NO (Ongoing) DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004613-34 | Sponsor Protocol Number: NordLOTS protocol 1.4 | Start Date*: 2008-03-14 | ||||||||||||||||
Sponsor Name:The Centre for Child and Adolescent Mental Health, Eastern and Southern Norway (R.BUP) | ||||||||||||||||||
Full Title: Nordic Longterm OCD treatment Study: A Nordic Multicenter treatment study evaluating a stepped care model based on the "Expert Clinical Guidelines". The study is performed with no sponsor from phar... | ||||||||||||||||||
Medical condition: Obsessive Compulsive Disorder | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Ongoing) DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002228-18 | Sponsor Protocol Number: AB-GEN-2013 | Start Date*: 2013-10-28 |
Sponsor Name:AB-BIOTICS S.A. | ||
Full Title: A randomized controlled clinical trial for assessing the effectiveness of pharmacogenetic information obtained with NEUROFARMAGEN in the treatment of patients with mental disorders | ||
Medical condition: Major depressive disorder schizophrenia Bipolar disorder obsessive-compulsive disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-005000-17 | Sponsor Protocol Number: CAFQ056A2225 | Start Date*: 2013-08-08 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, parallel-group proof of concept study to evaluate the effect of AFQ056 in obsessive compulsive disorder (OCD) patients resistant to Selective Seroton... | |||||||||||||
Medical condition: obsessive compulsive disorder (OCD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) CZ (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000175-86 | Sponsor Protocol Number: CN138-180 | Start Date*: 2017-04-07 |
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, | ||
Full Title: A 52-Week, Open-label, Multicenter Study of the Safety and Tolerability of Aripiprazole Flexibly Dosed in the Treatment of Children and Adolescents with Autistic Disorder | ||
Medical condition: Autistic disorder | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2013-001694-24 | Sponsor Protocol Number: D1050302 | Start Date*: 2014-03-11 | |||||||||||
Sponsor Name:SUNOVION PHARMACEUTICALS INC. | |||||||||||||
Full Title: A 104-WEEK, FLEXIBLE-DOSE, OPEN-LABEL, MULTICENTER, EXTENSION STUDY TO EVALUATE THE LONG-TERM SAFETY AND EFFECTIVENESS OF LURASIDONE IN PEDIATRIC SUBJECTS WITH SCHIZOPHRENIA AND SUBJECTS WITH IRRIT... | |||||||||||||
Medical condition: SCHIZOPHRENIA AND IRRITABILITY ASSOCIATED WITH AUTISTIC DISORDER | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Prematurely Ended) BG (Completed) Outside EU/EEA HU (Completed) GB (Completed) DE (Completed) PL (Completed) BE (Completed) FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001045-12 | Sponsor Protocol Number: APH205 | Start Date*: 2021-09-22 | |||||||||||
Sponsor Name:Asarina Pharma ApS | |||||||||||||
Full Title: A randomized, open-label, multicenter, phase 2 clinical trial to explore the safety and efficacy of sepranolone in pediatric and adult patients with Tourette Syndrome. | |||||||||||||
Medical condition: Tourette Syndrome | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003219-22 | Sponsor Protocol Number: LMS/SF/UH/0018 | Start Date*: 2014-01-27 | |||||||||||
Sponsor Name:Hertfordshire Partnership University NHS Foundation Trust [...] | |||||||||||||
Full Title: A randomised controlled feasibility trial comparing clinical and cost effectiveness of cognitive behavioural therapy (CBT) and selective serotonin reuptake inhibitors (SSRI) and their combination i... | |||||||||||||
Medical condition: Obsessive Compulsive Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002430-36 | Sponsor Protocol Number: AntibioTICS | Start Date*: 2012-07-02 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: Multicentre, randomised, double-blinded, placebo-controlled trial of efficacy of amoxicilline/clavulanic acid in patients affected by tic disorder colonized by GAS. No-proft stidy. | |||||||||||||
Medical condition: Chronic tic disorder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) ES (Ongoing) NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000867-21 | Sponsor Protocol Number: NGAM-13 | Start Date*: 2021-08-16 |
Sponsor Name:Octapharma Pharmazeutika Produktionsges.m.b.H. | ||
Full Title: A Superiority Study To Compare The Effect of Panzyga Versus Placebo in Patients with Pediatric Acute-onset Neuropsychiatric Syndrome | ||
Medical condition: Pediatric Acute-Onset Neuropsychiatric Syndrome (PANS). PANS is a research diagnosis given to patients who have an abrupt, dramatic onset of neuropsychiatric symptoms including obsessions/compulsio... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000612-26 | Sponsor Protocol Number: FINTOURPARK | Start Date*: 2011-09-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI CAGLIARI | |||||||||||||
Full Title: Open-label study on the use of Finasteride in prolonged treatment (4 years) of tics in Tourette's disease and Parkinson's disease in the pounding | |||||||||||||
Medical condition: Syndrome Gilles de la Tourette's disease Parkinosn Pounding | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000014-38 | Sponsor Protocol Number: THX-G18-001 | Start Date*: 2018-08-02 | |||||||||||
Sponsor Name:Therapix Biosciences Ltd. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo Controlled Proof of Concept Study to Evaluate the Safety, Tolerability and Efficacy of Daily Oral THX-110 in Treating Adults with Tourette Syndrome (“ENTOURAGE”) | |||||||||||||
Medical condition: Tourette Syndrome | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000564-42 | Sponsor Protocol Number: CANNA-TICS | Start Date*: 2017-06-14 | ||||||||||||||||
Sponsor Name:Hannover Medical School | ||||||||||||||||||
Full Title: A randomized multi-centre double-blind placebo controlled trial to demonstrate the efficacy and safety of nabiximols in the treatment of adults with chronic tic disorders (CANNA-TICS) | ||||||||||||||||||
Medical condition: Chronic tic disorders and Tourette syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-003466-33 | Sponsor Protocol Number: 1103-011 | Start Date*: 2013-05-17 | |||||||||||
Sponsor Name:Mental Health Services North Holland North | |||||||||||||
Full Title: Memantine Add-On Therapy to Clozapine | |||||||||||||
Medical condition: Cognitive functioning, severity of psychopathology and treatment response (positive symptoms and negative symptoms of schizophrenia), depressive symptoms, social cognition, obsessive-compulsive sy... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000342-32 | Sponsor Protocol Number: 248.642 | Start Date*: 2009-02-17 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: An open-label, flexible dose, follow-up study to evaluate safety and efficacy of oral pramipexole (0.0625-0.5 mg/day) for 24 weeks in children and adolescents (age 6-17 years) diagnosed with Touret... | |||||||||||||
Medical condition: Tourette's Syndrome | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) Outside EU/EEA | |||||||||||||
Trial results: View results |
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