- Trials with a EudraCT protocol (354)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
354 result(s) found for: Mental hospital.
Displaying page 1 of 18.
EudraCT Number: 2004-001981-41 | Sponsor Protocol Number: BALANCE Trial | Start Date*: 2005-01-24 | |||||||||||
Sponsor Name:UNIVERSITY OF OXFORD | |||||||||||||
Full Title: Bipolar Affective disorder: Lithium/ANti-Convulsant Evaluation | |||||||||||||
Medical condition: Maintenance treatment of bipolar disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000757-13 | Sponsor Protocol Number: RGH-MD-54 | Start Date*: 2016-06-07 | |||||||||||
Sponsor Name:Forest Laboratories LLC, an Allergan Affiliate | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter, Fixed-Dose Clinical Trial Evaluating the Efficacy, Safety and Tolerability of Cariprazine in Patients with Bipo... | |||||||||||||
Medical condition: Bipolar I Depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LT (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004990-10 | Sponsor Protocol Number: MF/UME01 | Start Date*: 2012-01-09 |
Sponsor Name:Sahlgrenska Academy | ||
Full Title: Double-blind placebo controlled study of the effects of OSU6162 on chronic fatigue in patients who suffered a mild traumatic brain injury | ||
Medical condition: Mental fatigue after traumatic brain injury | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
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: 2011-000925-60 | Sponsor Protocol Number: R1/11 | Start Date*: 2011-10-18 |
Sponsor Name:Kungälv Hospital | ||
Full Title: Effect of treatment with methylphenidate on mental fatigue (“brain fatigue”) and pain on persons who have suffered a traumatic brain injury or whip lash injury – a pilot study. | ||
Medical condition: Mental fatigue after traumatic brain injury or whip-lash injury | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002096-14 | Sponsor Protocol Number: MF115 | Start Date*: 2015-08-28 |
Sponsor Name:Sahlgrenska University Hospital | ||
Full Title: Examine whether treatment with methylphenidate facilitates work rehabilitation for persons with long-term pain and mental fatigue after traumatic brain injury. | ||
Medical condition: Long-term pain and mental fatigue after traumatic brain injury and work rehabilitation. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000756-98 | Sponsor Protocol Number: RGH-MD-53 | Start Date*: 2016-07-19 | |||||||||||
Sponsor Name:Forest Laboratories LLC, an Allergan Affiliate | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter, Fixed-Dose Clinical Trial Evaluating the Efficacy, Safety and Tolerability of Cariprazine in Patients with Bipo... | |||||||||||||
Medical condition: Bipolar I Depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) HR (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001650-29 | Sponsor Protocol Number: MF02/11 | Start Date*: 2011-12-19 |
Sponsor Name:A. Carlsson Research AB | ||
Full Title: TREATMENT OF MENTAL FATIGUE ("BRAIN FATIGUE") WITH THE DOPAMINERGIC STABILIZER OSU6162 AFTER STROKE AND MILD/MODERATE TRAUMATIC BRAIN INJURY– INCREASE OF PATIENT NUMBER | ||
Medical condition: Mental fatigue after stroke or mild to moderate head trauma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004460-63 | Sponsor Protocol Number: EXPO | Start Date*: 2019-07-01 | ||||||||||||||||
Sponsor Name:South London and Maudsley NHS Foundation Trust [...] | ||||||||||||||||||
Full Title: Extended-release Pharmacotherapy for Opioid Use Disorder (EXPO): An Open Label Randomised Controlled Trial of Injectable Depot Maintenance Buprenorphine versus Standard-Of-Care Oral Maintenance Opi... | ||||||||||||||||||
Medical condition: Opiod addiction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001017-16 | Sponsor Protocol Number: FARM9A8J83 | Start Date*: 2012-04-16 | ||||||||||||||||
Sponsor Name:IRCCS FONDAZIONE ISTITUTO NEUROLOGICO C. MONDINO | ||||||||||||||||||
Full Title: A randomized controlled trial of generic substitution of antiepileptic drugs | ||||||||||||||||||
Medical condition: Epilepsy or other diseases in which using: carbamazepine, lamotrigine, levetiracetam, oxcarbazepine, topiramate and valproate in mono or politerapy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004276-35 | Sponsor Protocol Number: PI-0290-2012 | Start Date*: 2014-10-10 | |||||||||||
Sponsor Name:Hospital Regional Universitario. IBIMA | |||||||||||||
Full Title: Phase II, Double-blind, randomized, 1-way cross-over, to investigate the effectiveness of the combination of ascorbic acid (vitamin C) and tocopherol (vitamin E) versus placebo for the treatment of... | |||||||||||||
Medical condition: The trial aims to treat depression. The incidence of major depression in the elderly accounts for between 3.6 and 4.8% and increases to 8 to 37.4% when depressive disorders in general is studied. B... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024632-42 | Sponsor Protocol Number: H9P-MC-LNBN | Start Date*: 2011-05-05 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: LY2216684 compared to Placebo as Adjunctive Therapy to SSRI in the Prevention of Symptom Re-emergence in Major Depressive Disorder | |||||||||||||
Medical condition: major depressive disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) SK (Completed) GR (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004349-34 | Sponsor Protocol Number: 202003 | Start Date*: 2020-06-17 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: Early mental response to hormonal treatment in transgender men | ||
Medical condition: Transsexualism | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002451-26 | Sponsor Protocol Number: 538264464328 | Start Date*: 2015-05-15 | |||||||||||
Sponsor Name:Department of Psychiatry, Helsinki University Central Hospital | |||||||||||||
Full Title: The effect of intranasal ketamine on suicidality in severely depressed and suicidal patients. Randomized, placebo-controlled study | |||||||||||||
Medical condition: Depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000420-34 | Sponsor Protocol Number: CHUB-NAC-Craving | Start Date*: 2018-11-27 | |||||||||||
Sponsor Name:Centre Hospitalier Universitaire Brugmann | |||||||||||||
Full Title: Efficacy of N-acetylcysteine on the craving symptoms of hospitalized patients with cocaine addiction. | |||||||||||||
Medical condition: Cocaine addiction | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023969-21 | Sponsor Protocol Number: 724 | Start Date*: 2011-10-28 | |||||||||||
Sponsor Name:Gateshead Health NHS Foundation Trust | |||||||||||||
Full Title: Vascular Augmentation of Late-life Unremitted Depression | |||||||||||||
Medical condition: Late-life (aged 50 or over) unremitted vascular depression. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000251-89 | Sponsor Protocol Number: 1042-0800 | Start Date*: 2014-10-22 | |||||||||||
Sponsor Name:Antwerp University Hospital | |||||||||||||
Full Title: A controlled double-blind crossover trial of ganaxolone in children with fragile X syndrome | |||||||||||||
Medical condition: behavioral problems in children with fragile X syndrome | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021142-21 | Sponsor Protocol Number: QUET-SON-2010 | Start Date*: 2010-09-23 | |||||||||||
Sponsor Name:Fundación Institut de Recerca de l' Hospital de la Santa Creu i Sant Pau | |||||||||||||
Full Title: ?Alteraciones del sueño en pacientes con depresión mayor resistente al tratamiento con inhibidores selectivos de la recaptación de serotonina: ensayo clínico, aleatorizado, abierto, de grupos paral... | |||||||||||||
Medical condition: Depresión mayor resistente a Inhibidores Selectivos de la Recaptación de serotonina, Código de clasificación de la CIE : F-33 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004509-29 | Sponsor Protocol Number: 2012-776 | Start Date*: 2015-11-03 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Antidepressant treatments during pregnancy and lactation: prediction of drug exposure through breastfeeding and evaluation of drug effect on the neonatal adaptation and the development of the youn... | |||||||||||||
Medical condition: depression | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006561-32 | Sponsor Protocol Number: OxyCog-01 | Start Date*: 2009-11-05 |
Sponsor Name:LWL University Hospital Bochum | ||
Full Title: Effects of intranasal application of oxytocin on empathy and mentalising in patients with psychotic disorders and severe personality disorders | ||
Medical condition: Schizophrenia, bipolar disorder, major depression, personality disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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