- Trials with a EudraCT protocol (20)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
20 result(s) found for: Anxiety neurosis.
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EudraCT Number: 2014-004475-23 | Sponsor Protocol Number: 47410 | Start Date*: 2016-10-05 | |||||||||||
Sponsor Name:Radboud University Nijmegen | |||||||||||||
Full Title: Enhancement of exposure therapy for social anxiety disorder with testosterone: A randomized clinical trial | |||||||||||||
Medical condition: Social Anxiety Disorder (Social Phobia) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005366-30 | Sponsor Protocol Number: Hovatta_Erkko_001 | Start Date*: 2016-09-05 | |||||||||||
Sponsor Name:University of Helsinki | |||||||||||||
Full Title: RESOLVING THE NEUROBIOLOGICAL MECHANISMS OF ANXIETY DISORDERS – BRAIN IMAGING SUB-STUDY | |||||||||||||
Medical condition: Social Anxiety disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004177-83 | Sponsor Protocol Number: 37202 | Start Date*: 2011-11-14 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Boosting the oxytocin system in acute trauma: The effectiveness of intranasal oxytocin treatments and stimulation of social support on preventing trauma related psychopathology | |||||||||||||
Medical condition: Posttraumatic Stress Disorder (PTSD) according to criteria in the DSM-IV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000426-62 | Sponsor Protocol Number: CHDR1203-E | Start Date*: 2013-04-10 | ||||||||||||||||
Sponsor Name:Centre for Human Drug Research | ||||||||||||||||||
Full Title: A randomized, double blind, placebo-controlled crossover study to investigate the effects of a selective serotonergic reuptake inhibitor on resting state fMRI in healthy volunteers. | ||||||||||||||||||
Medical condition: healthy volunteers 'depression, anxiety' | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-006228-19 | Sponsor Protocol Number: PTF3 | Start Date*: 2012-03-21 | |||||||||||
Sponsor Name:Psykiatrisk Center Ballerup | |||||||||||||
Full Title: The treatment of traumatized refugees with Setraline versus Venlafaxine - a randomized trial. | |||||||||||||
Medical condition: Post traumatic stress disorder (PTSD) Depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015538-30 | Sponsor Protocol Number: OXTsozphob | Start Date*: 2010-04-21 | |||||||||||
Sponsor Name:Rheinisch-Westfälisch Technische Hochschule Aachen | |||||||||||||
Full Title: Effect of intranasal oxytocin on social approach in patients with social phobia and healthy control | |||||||||||||
Medical condition: The effect of oxytocin is investigated in social processing of social phobic patient and healthy controls | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023007-10 | Sponsor Protocol Number: TF2010 | Start Date*: 2011-03-22 | |||||||||||
Sponsor Name:Uppsala university | |||||||||||||
Full Title: A neuroscience perspective on anxiety proneness - Sex differences, monoaminergic pathways and treatment response | |||||||||||||
Medical condition: Men and women diagnosed with DSM-IV social phobia (social anxiety disorder) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004153-40 | Sponsor Protocol Number: PTF5 | Start Date*: 2016-01-07 | |||||||||||
Sponsor Name:Competence Centre for Transcultural Psychiatry | |||||||||||||
Full Title: TREATMENT OF SLEEP DISTURBANCES IN TRAUMA-AFFECTED REFUGEES – A RANDOMISED CONTROLLED TRIAL | |||||||||||||
Medical condition: Posttraumatic Stress Disorder (PTSD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001288-58 | Sponsor Protocol Number: 40122 | Start Date*: 2012-05-21 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Boosting oxytocin after trauma: The effects of intranasal oxytocin administration on emotional and motivational brain processes in PTSD | |||||||||||||
Medical condition: Posttraumatic Stress Disorder (PTSD) according to criteria in the DSM-IV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004982-41 | Sponsor Protocol Number: 14865A | Start Date*: 2013-11-11 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Interventional, randomised, double-blind, parallel-group, placebo-controlled, flexible-dose study of brexpiprazole as adjunctive treatment to paroxetine or sertraline in adult patients suffering... | |||||||||||||
Medical condition: Post-traumatic stress disorder (PTSD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Prematurely Ended) IT (Prematurely Ended) FI (Prematurely Ended) SE (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022460-12 | Sponsor Protocol Number: MVH-03 | Start Date*: 2011-03-23 | ||||||||||||||||||||||||||
Sponsor Name:Herlev Hospital | ||||||||||||||||||||||||||||
Full Title: The effect of melatonin on depression, anxiety, cogntive function and sleep disturbances in breast cancer patients | ||||||||||||||||||||||||||||
Medical condition: Depression Anxiety Postoperative cognitive dysfunction Sleep disturbances | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020170-42 | Sponsor Protocol Number: 12708A | Start Date*: 2012-10-05 | ||||||||||||||||
Sponsor Name:H. Lundbeck A/S | ||||||||||||||||||
Full Title: An open-label study evaluating the Pharmacokinetics and Tolerability of Lu AA21004 in connection with multiple oral dosing of Lu AA21004 in child and adolescent patients with a DSM-IV-TRTM diagnosi... | ||||||||||||||||||
Medical condition: DSM-IV-TRTM diagnosed Depressive or Anxiety Disorder | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003404-12 | Sponsor Protocol Number: CL2-20098-075 | Start Date*: 2013-02-12 | ||||||||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | ||||||||||||||||||
Full Title: Pharmacokinetics and safety of agomelatine in children (from 7 to less than 12 years) and adolescents (from 12 to less than 18 years) with Depressive or Anxiety Disorder. An open-labelled, multice... | ||||||||||||||||||
Medical condition: Depressive or Anxiety Disorder | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) SE (Completed) HU (Completed) EE (Completed) RO (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-003658-47 | Sponsor Protocol Number: F02207 GE 3 03 | Start Date*: 2006-11-21 | |||||||||||
Sponsor Name:Pierre Fabre Médicament - IRPF | |||||||||||||
Full Title: Exploratory study of the efficacy and safety of flexible doses of Milnacipran and Venlafaxine administered in out patients with Major Depressive Disorder. | |||||||||||||
Medical condition: Major Depressive Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003597-10 | Sponsor Protocol Number: CRH103390 | Start Date*: 2006-11-04 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development | |||||||||||||
Full Title: Study CRH103390: A 12 Week Flexible Dose Study of GW876008, Placebo and Active Control (Paroxetine) in the Treatment of Social Anxiety Disorder (SocAD) | |||||||||||||
Medical condition: Social Anxiety Disorder (SocAD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005476-41 | Sponsor Protocol Number: MMHSCT1096 | Start Date*: 2012-05-18 | |||||||||||
Sponsor Name:Manchester Mental Health and Social Care Trust | |||||||||||||
Full Title: Ketamine augmentation of ECT to improve outcomes in depression | |||||||||||||
Medical condition: Depressive disorder requiring treatment with electroconvulsive treatment (ECT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004132-33 | Sponsor Protocol Number: D1050304 | Start Date*: 2013-05-02 | |||||||||||
Sponsor Name:Sunovion Pharmaceuticals Inc. | |||||||||||||
Full Title: A Randomized, 6-Week, Double-Blind, Placebo-Controlled, Flexible-Dose, Parallel-Group Study of Lurasidone for the Treatment of Major Depressive Disorder with Mixed Features (Protocol No D1050304) | |||||||||||||
Medical condition: Major Depressive Disorder (MDD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005457-25 | Sponsor Protocol Number: PCN-101-21 | Start Date*: 2021-08-30 | |||||||||||
Sponsor Name:Perception Neuroscience, Inc | |||||||||||||
Full Title: A randomized, placebo-controlled, double-blind study to assess the safety and efficacy of intravenous PCN-101 in treatment-resistant depression | |||||||||||||
Medical condition: Treatment-resistant depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001997-70 | Sponsor Protocol Number: EXCELLENCE/0421/0543v1 | Start Date*: 2022-11-16 | ||||||||||||||||||||||||||
Sponsor Name:University of Cyprus | ||||||||||||||||||||||||||||
Full Title: Efficacy of Ketamine for the Prevention of Relapse in Patients with Opioid-Use Disorders (OUD) | ||||||||||||||||||||||||||||
Medical condition: Methadone and buprenorphine comprise a first-line, evidence-based opioid substitution treatment (OST) for OUD patients. Unfortunately, retention and adherence to OST treatment is currently a major ... | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: CY (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005037-32 | Sponsor Protocol Number: PSIKET_002CZE | Start Date*: 2021-09-22 | |||||||||||
Sponsor Name:Národní ústav duševního zdraví | |||||||||||||
Full Title: Psilocybin - a strategy of rapid antidepressant response in depression comorbid with cancer, a randomized double-blind study with the possibility of entering open extension. | |||||||||||||
Medical condition: Depressive disorder comorbid with cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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