- Trials with a EudraCT protocol (211)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
211 result(s) found for: Antidepressants.
Displaying page 1 of 11.
EudraCT Number: 2008-004167-19 | Sponsor Protocol Number: 658321 | Start Date*: 2010-01-11 |
Sponsor Name:GGz Nijmegen | ||
Full Title: The effectiveness of antidepressants and psychological intervention in treating conversion disorder, motor type: a randomized placebo controlled clinical trial. | ||
Medical condition: Conversion disorder, motor type. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011893-13 | Sponsor Protocol Number: 1234567899 | Start Date*: 2010-04-29 |
Sponsor Name:Isala Klinieken | ||
Full Title: Adherence of antidepressants during pregnancy | ||
Medical condition: Pregnant women with psychiatric morbidity and an strong indication for using antidepressants | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004210-26 | Sponsor Protocol Number: 14/0647 | Start Date*: 2016-11-22 | |||||||||||
Sponsor Name:PRIMENT Clinical Trials Unit, UCL | |||||||||||||
Full Title: A Phase IV double blind multi-site, individually randomised parallel group controlled trial investigating the use of citalopram, sertraline, fluoxetine and mirtazapine in preventing relapse in pati... | |||||||||||||
Medical condition: Depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000043-74 | Sponsor Protocol Number: PNAS0122 | Start Date*: 2023-07-27 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Defining and predicting neonatal inadaptation after gestational exposure to antidepressants: longitudinal exploratory analysis of psychoneuroendocrine risk factors and complications | ||
Medical condition: major depressive disorder poor neonatal adaptation syndrome (after antidepressant use during pregnancy) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002782-19 | Sponsor Protocol Number: 3111-301-001 | Start Date*: 2019-10-24 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF CARIPRAZINE AS AN ADJUNCT TO ANTIDEPRESSANTS IN THE TREATMENT OF PATIENTS WITH MAJOR DEPRESSIVE DISORDER WHO HAVE HAD AN INADEQUATE RESPONSE TO ANTIDEPRE... | |||||||||||||
Medical condition: Major Depressive Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) BG (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000090-23 | Sponsor Protocol Number: UoB1651 | Start Date*: 2013-06-19 | |||||||||||
Sponsor Name:University of Bristol | |||||||||||||
Full Title: Mirtazapine added to SSRIs for treatment resistant depression in primary care: a placebo controlled randomised controlled trial | |||||||||||||
Medical condition: Treatment resistant depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002727-18 | Sponsor Protocol Number: Lisette-2 | Start Date*: 2011-10-24 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: The effects of switching antidepressants on endoxifen exposure | |||||||||||||
Medical condition: Breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001361-32 | Sponsor Protocol Number: 14571A | Start Date*: 2013-04-29 | ||||||||||||||||||||||||||
Sponsor Name:H. Lundbeck A/S | ||||||||||||||||||||||||||||
Full Title: Interventional, randomised, double-blind, parallel-group, placebo-controlled, fixed-dose study to evaluate the efficacy and safety of brexpiprazole (1 and 3 mg/day) as adjunctive treatment in el... | ||||||||||||||||||||||||||||
Medical condition: Major Depressive Disorder | ||||||||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) LT (Prematurely Ended) FI (Prematurely Ended) SK (Prematurely Ended) EE (Prematurely Ended) BG (Prematurely Ended) GB (Prematurely Ended) PL (Prematurely Ended) RO (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-005531-17 | Sponsor Protocol Number: Xe-01 | Start Date*: 2007-05-08 |
Sponsor Name:Klinik für Anästhesiologie Universitätsklinikum Aachen | ||
Full Title: Xenon als Antidepressivum | ||
Medical condition: Major depressive disorder and recurrent mayor depressive disorder (ICD 10 F32.2 and 33.3) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003370-27 | Sponsor Protocol Number: DMFMRI201303 | Start Date*: 2014-09-25 |
Sponsor Name:Rainer Rupprecht, Klinik und Poliklinik für Psychiatrie und Psychotherapie der Universität Regensburg am Bezirksklinikum | ||
Full Title: Functional MRI (fMRI) after challenge and treatment with antidepressants and their relation to the clinical course, to the Hypothalamus-Hypophysis-Adrenocortical Axis and the colon microbiome | ||
Medical condition: Major Depressive Disorder is a chronic stress related disorder characterized by depressed mood and by vegetative and cognitive symptoms. Moreover, genetic, neuroendocrine and neurochemical biomarke... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-005100-99 | Sponsor Protocol Number: TYH2018307 | Start Date*: 2018-06-14 |
Sponsor Name:Helsinki University and University Hospital | ||
Full Title: Pharmacoepidemiology and pharmacogenetics of antidepressant treatment for depressive disorders (PEGAD) | ||
Medical condition: Depression (ICD-10 F32 and F33). Clinically diagnosed depression (F32-33), with symptom severity equaling or exceeding score 10 in the Patient Health Questionnaire (PHQ-9) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003164-31 | Sponsor Protocol Number: 3111-302-001 | Start Date*: 2019-08-15 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF CARIPRAZINE AS AN ADJUNCT TO ANTIDEPRESSANTS IN THE TREATMENT OF PATIENTS WITH MAJOR DEPRESSIVE DISORDER WHO HAVE HAD AN INADEQUATE RESPONSE TO ANTIDEPRE... | |||||||||||||
Medical condition: Major Depressive Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SK (Completed) PL (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004184-36 | Sponsor Protocol Number: UKER-AN-HS-01 | Start Date*: 2016-01-05 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Prospective, randomised, double-blind, placebo-controlled, single centre phase IIa clinical trial to investigate the safety and tolerability as well as the impact of a substitution of sexual hormon... | |||||||||||||
Medical condition: Substitution of sexual hormones in adult females with anorexia nervosa | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001683-29 | Sponsor Protocol Number: 61393215MDD2001 | Start Date*: 2019-09-27 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: Double-Blind, Placebo-Controlled, Multi-Center Study Investigating the Efficacy, Safety, and Tolerability of JNJ-61393215 as Adjunctive Treatment in Adults with Major Depressive Disorder with Anxio... | |||||||||||||
Medical condition: Adjunctive Treatment in Adults with Major Depressive Disorder with Anxious Distress with Suboptimal Response to Standard Antidepressants | |||||||||||||
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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: 2006-000105-38 | Sponsor Protocol Number: 04/11/02 | Start Date*: 2006-08-04 |
Sponsor Name:King's College London (IOP) | ||
Full Title: A definitive multi-centre pragmatic randomised controlled double-blind trial of the clinical and cost effectiveness of mirtazapine and sertraline versus placebo for the treatment of depression in d... | ||
Medical condition: Depression in dementia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011582-88 | Sponsor Protocol Number: 41470956 | Start Date*: 2009-05-28 | |||||||||||
Sponsor Name:St James Hospital | |||||||||||||
Full Title: The differential effects of donepezil and placebo on EEG/ ERP measures and fMRI in mild cognitive impairment and elderly controls | |||||||||||||
Medical condition: Amnestic Mild cognitive Impairment (aMCI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003664-25 | Sponsor Protocol Number: 11323 | Start Date*: 2023-12-21 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: The impact of gender differences in P-glycoprotein function measured with [18F]MC225 and PET | ||
Medical condition: Gender, healthy volunteers | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005194-30 | Sponsor Protocol Number: P-AD337-021 | Start Date*: 2006-06-12 |
Sponsor Name:Arakis Ltd. | ||
Full Title: A multi-centre, randomised, double-blind, placebo controlled, parallel group exploratory study to investigate the efficacy, safety and tolerability of AD 337 in the treatment of fibromyalgia in fem... | ||
Medical condition: Fibromyalgia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017458-11 | Sponsor Protocol Number: DEP-HOM | Start Date*: 2010-06-10 |
Sponsor Name:Institute for Social Medicine, Epidemiology, and Health Economics, Charité Berlin | ||
Full Title: Homeopathy for Depression: a randomized, four-armed, partial double-blind study. | ||
Medical condition: F32.1 Moderate Depressive Episode | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-023446-70 | Sponsor Protocol Number: | Start Date*: 2011-07-22 |
Sponsor Name:Med. Univ. Wien, Univ. Klinik für Psychiatrie und Psychotherapie | ||
Full Title: Neural, Genetic, and Peripheral Correlates of SSRI Pharmaco-Response | ||
Medical condition: Major Depressive Disorder (MDD) remains to be under-recognized and under-treated, though it is amongst the leading causes of disease burden worldwide. Despite the proven efficacy of modern antidepr... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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