- Trials with a EudraCT protocol (286)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
286 result(s) found for: Behavioral Treatment.
Displaying page 1 of 15.
EudraCT Number: 2009-010965-22 | Sponsor Protocol Number: NF1-SIMCODA | Start Date*: 2009-09-29 |
Sponsor Name:Erasmus MC - Department of Pediatrics | ||
Full Title: The effect of long-term simvastatin treatment on cognitive function and daily life in children with Neurofibromatosis 1: a one year randomized controlled trial | ||
Medical condition: Neurofibromatosis 1 | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001560-35 | Sponsor Protocol Number: 2358 | Start Date*: 2016-04-07 |
Sponsor Name:Brain Center Rudolf Magnus, University Medical Center Utrecht, Department of Psychiatry, Utrecht , the Netherlands | ||
Full Title: Bumetanide in Autism Medication and BIomarker study | ||
Medical condition: Autism Spectrum Disorder | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005177-23 | Sponsor Protocol Number: N01395 | Start Date*: 2012-09-27 | |||||||||||
Sponsor Name:UCB Pharma SA | |||||||||||||
Full Title: An Open-Label, Multicenter, Single-Arm Study to Evaluate the Reduction in Nonpsychotic Behavioral Side Effects in Subjects with Epilepsy Switching from Levetiracetam to Brivaracetam due to Nonpsych... | |||||||||||||
Medical condition: Nonpyschotic Behavioural Side Effects in Subjects With Epilepsy | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005111-40 | Sponsor Protocol Number: CN138-178 | Start Date*: 2017-04-07 |
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc | ||
Full Title: A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Flexible- Dosed Parallel-Group Study 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: 2010-023941-31 | Sponsor Protocol Number: ETON | Start Date*: 2011-05-20 |
Sponsor Name:Charité Universitätsmedizin Berlin | ||
Full Title: Effects of EGCG (Epigallocatechin Gallate) in Chorea Huntington | ||
Medical condition: Huntington´s Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000767-28 | Sponsor Protocol Number: 20061 | Start Date*: 2006-09-29 |
Sponsor Name:Vienna Medical University | ||
Full Title: Standardisierte Verlaufsbeobachtung von Patienten mit intrathekalem S(+)-Ketamin | ||
Medical condition: Intrathecal S(+)-ketamine is a potent option in the treatment of chronic severe neuropathic pain in cancer patients refractory to conventional therapeutic strategies (Benrath et al. 2005). However,... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004325-16 | Sponsor Protocol Number: RC31/16/8407 | Start Date*: 2016-12-22 |
Sponsor Name:University Hospital of Toulouse | ||
Full Title: Long term evaluation of infants aged from 3 to 4 years old included in the OTBB2 study (repeated administrations of oxytocin in infants with PWS aged from 0 to 6 months) and comparison with not tre... | ||
Medical condition: Prader Willi Syndrom | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001989-38 | Sponsor Protocol Number: IMCRELA | Start Date*: 2021-07-08 | |||||||||||
Sponsor Name:Facultad de medicina y ciencias de la salud de la Universidad Católica de Valencia | |||||||||||||
Full Title: IMPACT OF THE COMBINED TREATMENT OF THE LIPOSOMATED POLYPHENOLS CÚRCULA AND RESVERATROL® WITH DUTASTERIDE, IN THE CLINICAL IMPROVEMENT OF PATIENTS WITH ALS TREATED WITH RILUZOLE | |||||||||||||
Medical condition: Amyotrophic Lateral Sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004444-19 | Sponsor Protocol Number: CRIT124D2201 | Start Date*: 2016-04-05 | |||||||||||
Sponsor Name:Novartis Pharmaceutical corporation | |||||||||||||
Full Title: An open-label, behavioral-treatment-controlled evaluation of the effects of extended release methylphenidate (Ritalin® LA) on the frequency of cytogenetic abnormalities in children 6 - 12 years of ... | |||||||||||||
Medical condition: To determine whether the administration of extended-release methylphenidate in treatment-naïve children with ADHD affects the frequency of chromosomal abnormalities. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
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: 2014-000586-45 | Sponsor Protocol Number: S56327 | Start Date*: 2014-05-08 | |||||||||||
Sponsor Name:KU Leuven | |||||||||||||
Full Title: Oxytocin-based pharmacotherapy for Autism Spectrum Disorders: Investigating the neural and behavioral effects of a promising intervention approach | |||||||||||||
Medical condition: Young male adults with Autism Spectrum Disorders (18-30 years) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003068-47 | Sponsor Protocol Number: UROBOTOX 1 | Start Date*: 2005-09-22 |
Sponsor Name:Region Skåne, Universitetssjukhuset i Lund, Urologiska kliniken | ||
Full Title: Behandling med botulinumtoxin vid neurogen blåsfunktionsstörning | ||
Medical condition: The trial addresses patients with severe symptoms of neurogenic detrusor overactivity (urgency and/or urge incontinence). Eligible are those patients who have failed conservative treatment such as ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022511-18 | Sponsor Protocol Number: X04 | Start Date*: 2011-04-05 | |||||||||||
Sponsor Name:Albert-Ludwig University Freiburg, Laboratory for Biological and Personality Psychology | |||||||||||||
Full Title: Behavioral effects and neural correlates of oxytocin on social attention [Verhaltenseffekte und neuronales Korrelat von Oxytocin im Kontext sozialer Aufmerksamkeit] | |||||||||||||
Medical condition: subjects with autism spectrum disorder and neurotypical controls | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003563-26 | Sponsor Protocol Number: NL74799.018.20 | Start Date*: 2020-10-15 |
Sponsor Name:TNO | ||
Full Title: Reconsolidation: a new intervention for traumatized healthcare workers. | ||
Medical condition: Post-traumatic stress disorder. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006886-18 | Sponsor Protocol Number: ALK21-014 | Start Date*: 2007-06-04 | |||||||||||
Sponsor Name:Alkermes Inc | |||||||||||||
Full Title: Efficacy and Safety of Vivitrol® in Adults Completing Inpatient Treatment for Alcohol Dependence | |||||||||||||
Medical condition: Alcohol Dependence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004024-11 | Sponsor Protocol Number: 60-60600-97-103 | Start Date*: 2014-07-23 | |||||||||||
Sponsor Name:Academic Psychiatric Center - AMC-UvA | |||||||||||||
Full Title: New pharmacotherapeutic treatment options for crack-cocaine dependent people in the Netherlands: A double-blind, placebo-controlled randomized feasibility study of sustained release dexamphetamine | |||||||||||||
Medical condition: cocaine dependence (according DSM-IV) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000829-55 | Sponsor Protocol Number: PSILO4ALCO | Start Date*: 2020-12-16 | ||||||||||||||||
Sponsor Name:Psychiatric Centre Copenhagen | ||||||||||||||||||
Full Title: Can a one-off administration of psilocybin reduce alcohol intake in patients with alcohol use disorder? A randomized, double-blinded, placebo-controlled clinical trial. | ||||||||||||||||||
Medical condition: Alcohol Use Disorder | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000208-41 | Sponsor Protocol Number: TV1380-COA-201 | Start Date*: 2013-09-17 | |||||||||||
Sponsor Name:Teva Pharmaceutical Industries Ltd. | |||||||||||||
Full Title: A 12-week, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Once-Weekly Intra-Muscular Injections of TV-1380 (150 mg/week or 30... | |||||||||||||
Medical condition: Treatment for Facilitation of Abstinence in Cocaine-Dependent Subjects | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000647-32 | Sponsor Protocol Number: PRIOTAB | Start Date*: 2014-10-22 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: Investigation of the efficacy of degarelix as an acute treatment for patients with pedophilic disorder to reduce the risk for sexual child molestation: a prospective, randomized, double blind, and ... | ||
Medical condition: Pedophilia acccording to DSM-5 (F65.4) | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001650-94 | Sponsor Protocol Number: 191622-133 | Start Date*: 2013-08-06 | |||||||||||
Sponsor Name:Allergan Limited | |||||||||||||
Full Title: An Exploratory Study of the Safety and Efficacy of BOTOX® for the Treatment of Premature Ejaculation | |||||||||||||
Medical condition: Premature Ejaculation | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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