- Trials with a EudraCT protocol (1,476)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (24)
1,476 result(s) found for: Depression.
Displaying page 38 of 74.
EudraCT Number: 2019-000821-37 | Sponsor Protocol Number: O3NPIQ | Start Date*: 2019-12-10 | |||||||||||
Sponsor Name:Bernardino Clavo - Hospital Universitario de G. C. Dr. Negrín | |||||||||||||
Full Title: Effectiveness and cost-effectiveness of Ozone therapy in patients with pain secondary to chemotherapy-induced peripheral neuropathy. Randomized, triple-blind clinical trial. | |||||||||||||
Medical condition: Pain secondary to chemotherapy-induced peripheral neuropathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002678-29 | Sponsor Protocol Number: ANAVEX2-73-PDD-EP-001 | Start Date*: 2019-12-05 | ||||||||||||||||
Sponsor Name:Anavex Life Sciences Corp. | ||||||||||||||||||
Full Title: Open Label Extension Study for Patients with Parkinson’s Disease with Dementia Previously Enrolled in ANAVEX2-73-PDD-001 Study for Continued Safety Assessment | ||||||||||||||||||
Medical condition: Cognition in Parkinson’s Disease with Dementia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003638-40 | Sponsor Protocol Number: XTL B07-001 | Start Date*: 2008-01-08 | |||||||||||
Sponsor Name:XTL Development Inc. | |||||||||||||
Full Title: A Double-blind, Randomized, Placebo-controlled, Parallel, Multicenter Study of the Safety and Efficacy of Two Dosages of Bicifadine SR in Adult Outpatients with Chronic Neuropathic Pain Associated ... | |||||||||||||
Medical condition: Chronic neuropathic pain in patients with diabetic peripheral neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004937-15 | Sponsor Protocol Number: BNC210.006 | Start Date*: 2015-04-16 | |||||||||||
Sponsor Name:BIONOMICS LIMITED | |||||||||||||
Full Title: A randomized, double-blinded, placebo and lorazepam-controlled, four-way crossover, Phase II study to evaluate the effects of single oral administration of BNC210 on brain activity changes captured... | |||||||||||||
Medical condition: Generalized Anxiety Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002858-36 | Sponsor Protocol Number: FIM-DON-2017-01 | Start Date*: 2018-09-19 | |||||||||||
Sponsor Name:FIMABIS Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina Y Salud | |||||||||||||
Full Title: STUDY OF THE EFFECTIVENESS AND CEREBRAL REORGANIZATION AFTER TREATMENT COMBINED WITH DONEPEZILO, INTENSIVE REHABILITATION AND TRANSCRANEAL DIRECT CURRENT STIMULATION IN POSTSTROKE CHRONIC AFASIA | |||||||||||||
Medical condition: Chronic poststroke aphasia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019858-41 | Sponsor Protocol Number: CR100101/CO15570 | Start Date*: 2011-02-09 | |||||||||||
Sponsor Name:Avraham Pharmaceuticals Ltd. | |||||||||||||
Full Title: A 6-month prospective, multi-center, double-blind, placebo-controlled, randomized, adaptive-trial-design study to evaluate the safety and efficacy of 80mg b.i.d. ladostigil in patients with mild to... | |||||||||||||
Medical condition: Patient with mild to moderate Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005524-15 | Sponsor Protocol Number: ELND005-AG251 | Start Date*: 2013-09-03 |
Sponsor Name:Elan Pharma International Ltd | ||
Full Title: A 36-Week Safety Extension Study of Oral ELND005 for Treatment of Agitation and Aggression in Patients With Moderate to Severe Alzheimer's Disease. | ||
Medical condition: Agitation and Aggression in Moderate to severe Alzheimer's Disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-002285-76 | Sponsor Protocol Number: 1111-1155-9921 | Start Date*: 2014-12-04 | |||||||||||
Sponsor Name:Hvidovre University Hospital | |||||||||||||
Full Title: The Effects of Liraglutide in Patients With Insulin Pump Treated Type 1 Diabetes: A Randomized, Placebo-Controlled Trial. The Lira Pump Trial. | |||||||||||||
Medical condition: Type 1 Diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000998-20 | Sponsor Protocol Number: DRO/IV-2016-ART-02 | Start Date*: 2016-06-08 |
Sponsor Name:BIOIBÉRICA S.A | ||
Full Title: Double-Blind, Randomised, Placebo-Controlled Clinical Trial to Evaluate the Efficacy and Safety of the Combination of Chondroitin Sulphate and Glucosamine Hydrochloride in Patients with Hand Osteoa... | ||
Medical condition: symptomatic hand osteoarthritis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001021-10 | Sponsor Protocol Number: SAHL1011 | Start Date*: 2018-08-06 | |||||||||||
Sponsor Name:Sahlgrenska University Hospital | |||||||||||||
Full Title: Brodalumab in a randomised, open, phase IV study evaluating clinical efficacy in psoriasis patients switching from TNF-alpha inhibitor treatment | |||||||||||||
Medical condition: Moderate to severe plaque psoriasis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005405-78 | Sponsor Protocol Number: 2011430 | Start Date*: 2012-02-01 | ||||||||||||||||
Sponsor Name:Steen Bendix Haugaard | ||||||||||||||||||
Full Title: Adding liraglutide to the backbone therapy of biguanide in patients with coronary artery disease and newly diagnosed type-2 diabetes | ||||||||||||||||||
Medical condition: Patients suffering of both Type 2 diabetes mellitus and coronary artery disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015537-67 | Sponsor Protocol Number: 2009-08-17 | Start Date*: 2009-11-23 | |||||||||||
Sponsor Name:Universitätsmedizin der Johannes Gutenberg-Universität Mainz | |||||||||||||
Full Title: Untersuchung der Wirksamkeit und Sicherheit von Vareniclin in der Postakutbehandlung der Alkoholabhängigkeit - eine prospektive, bizentrische, doppelblinde, placebokontrollierte, randomisierte Phas... | |||||||||||||
Medical condition: Alcohol dependence | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001115-39 | Sponsor Protocol Number: GON2014/05 | Start Date*: 2015-12-29 | |||||||||||
Sponsor Name:Barts Health NHS Trust | |||||||||||||
Full Title: A phase IV single-blind placebo-controlled cross-over study to investigate the efficacy of greater occipital nerve block with local anaesthetic and steroid in patients with chronic migraine. | |||||||||||||
Medical condition: Chronic migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001849-41 | Sponsor Protocol Number: DOX-101 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:Leids Universitair Medisch Centrum (LUMC) | |||||||||||||
Full Title: Two-part, Randomized, Placebo-controlled, Repeated Stepped Infusion Dose Study of the Pharmacodynamics of Doxapram when Co-administered with Opioids (Protocol – doxapram-101). | |||||||||||||
Medical condition: acute respiratory insufficiency, including such conditions as opioid and anesthetic-induced respiratory depression, post-anesthetic atelectasis, and central apneas (e.g., apnea of prematurity). | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004586-41 | Sponsor Protocol Number: CHUBX2012/16 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Cognitive remediation in Attention Deficit Disorder with or without Hyperactivity (ADHD) children : Comparison between three therapeutic strategies : cognitive remediation with a virtual classroom ... | |||||||||||||
Medical condition: Attention Deficit Disorder with or without Hyperactivity | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001025-53 | Sponsor Protocol Number: 109MS405 | Start Date*: 2015-03-05 | ||||||||||||||||
Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
Full Title: A Multicenter, Open-Label Study to Evaluate Fatigue in Subjects With Relapsing Remitting Multiple Sclerosis During Treatment With Tecfidera® (Dimethyl Fumarate) Gastro-Resistant Hard Capsule | ||||||||||||||||||
Medical condition: Relapsing-Remitting Multiple Sclerosis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000323-86 | Sponsor Protocol Number: N/A | Start Date*: 2017-05-05 | ||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||
Full Title: A randomised, parallel group, double blind, placebo controlled, add on clinical trial to investigate whether the lithium mimetic, ebselen, can reduce symptoms of hypomania and mania in bipolar pati... | ||||||||||||||||||
Medical condition: Patients with bipolar disorder meeting DSM-5 criteria for hypomania or mania | ||||||||||||||||||
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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: 2004-003927-11 | Sponsor Protocol Number: A7501008 | Start Date*: 2005-08-04 | |||||||||||
Sponsor Name:NV Organon | |||||||||||||
Full Title: A Phase 3, Randomized, Placebo-Controlled, Double-Blinded Trial Evaluating the Safety and Efficacy of Asenapine in Subjects Continuing Lithium or ValproicAcid/Divalproex Sodium for the Treatment of... | |||||||||||||
Medical condition: Bipolar 1 Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002599-86 | Sponsor Protocol Number: POF1 | Start Date*: 2009-03-03 | |||||||||||
Sponsor Name:Guy's and St Thomas Foundation NHS Trust [...] | |||||||||||||
Full Title: A prospective open randomised controlled trial of women diagnosed with premature ovarian failure (POF) to investigate the effects of active treatment with HRT (hormone replacement therapy) or COCP ... | |||||||||||||
Medical condition: Premature ovarian failure | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000763-42 | Sponsor Protocol Number: A5361020 | Start Date*: 2008-09-05 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 3, RANDOMIZED, DOUBLE-BLIND, PARALLEL GROUP, 10-WEEK PLACEBO CONTROLLED FIXED DOSE STUDY OF PD 0332334 AND PAROXETINE EVALUATING THE EFFICACY AND SAFETY OF PD 0332334 FOR THE TREATMENT OF G... | |||||||||||||
Medical condition: Generalized Anxiety Disorder (GAD). | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
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