- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
15 result(s) found for: Trazodone.
Displaying page 1 of 1.
EudraCT Number: 2006-000216-24 | Sponsor Protocol Number: 2006-Traz_insomnia | Start Date*: 2006-04-21 |
Sponsor Name:University of Bristol | ||
Full Title: Serotonin sensitivity in insomnia: a placebo-controlled crossover study of sleep after 5HT2 blockade in primary insomnia. | ||
Medical condition: Primary insomnia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001166-42 | Sponsor Protocol Number: 152PO17433 | Start Date*: 2018-11-27 | |||||||||||
Sponsor Name:Aziende Chimiche Riunite Angelini Francesco ACRAF S.p.A (Angelini S.p.A.) | |||||||||||||
Full Title: A multi-centre, randomized, parallel-group, single blind Phase II trial to evaluate the pharmacokinetics and PKPD relationship of trazodone after single and repeated oral doses in children from 2 t... | |||||||||||||
Medical condition: Insomnia in children and adolescents with autism, intellectual disability or ADHD | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002711-25 | Sponsor Protocol Number: 039SC04253 | Start Date*: 2005-08-01 | |||||||||||
Sponsor Name:ANGELINI | |||||||||||||
Full Title: DOSE-FINDING STUDY OF TRAZODONE IN THE TREATMENT OF PATIENTS WITH PRIMARY INSOMNIA | |||||||||||||
Medical condition: TREATMENT OF THE INSOMNIA | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) SK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000133-12 | Sponsor Protocol Number: 039(1)PO16357 | Start Date*: 2018-10-26 | |||||||||||||||||||||
Sponsor Name:Angelini S.p.A. | |||||||||||||||||||||||
Full Title: Efficacy and safety of Fixed-Dose Combination (FDC) products containing trazodone and gabapentin in patients affected by painful diabetic neuropathy: randomized, controlled, dose finding study. | |||||||||||||||||||||||
Medical condition: Painful diabetic neuropathy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) GB (Completed) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-005007-12 | Sponsor Protocol Number: 039(C)MD21046 | Start Date*: 2023-02-17 | |||||||||||
Sponsor Name:Angelini Pharma S.p.A. | |||||||||||||
Full Title: Efficacy of Trazodone Once-a-Day for treatment of Major Depressive Disorder in patients with breast cancer. | |||||||||||||
Medical condition: Major Depressive Disorder | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005878-37 | Sponsor Protocol Number: 039(C)SC11063 | Start Date*: 2012-06-05 | |||||||||||||||||||||
Sponsor Name:ANGELINI | |||||||||||||||||||||||
Full Title: A randomized, double-blind study comparing the efficacy and safety of trazodone OAD and venlafaxine XR in the treatment of patients with Major Depressive Disorder | |||||||||||||||||||||||
Medical condition: Major Depressive Disorder | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) AT (Completed) CZ (Completed) ES (Completed) SK (Completed) RO (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002772-27 | Sponsor Protocol Number: 039(B)PO16143 | Start Date*: 2017-03-20 | |||||||||||||||||||||
Sponsor Name:Angelini S.p.A. | |||||||||||||||||||||||
Full Title: Efficacy and safety of low doses of trazodone in patients affected by painful diabetic neuropathy: randomized, controlled, pilot study. | |||||||||||||||||||||||
Medical condition: Painful diabetic neuropathy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) HU (Completed) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000099-41 | Sponsor Protocol Number: AC18082 | Start Date*: 2019-10-02 | |||||||||||
Sponsor Name:University of Edinburgh [...] | |||||||||||||
Full Title: Motor Neurone Disease Systematic Multi-arm Adaptive Randomised Trial (MND-SMART) | |||||||||||||
Medical condition: Motor Neurone Disease | |||||||||||||
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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: 2007-002140-24 | Sponsor Protocol Number: CSC/Trazo-01/07 | Start Date*: 2007-07-12 | |||||||||||
Sponsor Name:CSC Pharmaceuticals Handels GmbH. | |||||||||||||
Full Title: Open-label, Multicenter Clinical Study of Dose-dependent Efficacy and Safety of Trazodone Hydrochloride in Patients wirh Major Depressive Disorder ans Pain (TIPAD Study) | |||||||||||||
Medical condition: Major Depression Disorder associated with painful physical symptoms | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004936-31 | Sponsor Protocol Number: ICADTSIII | Start Date*: 2014-05-28 |
Sponsor Name:Ministry of Infrastructure and the Environment | ||
Full Title: Establish limits for fitness to drive with prolonged use of ICADTS class III medication | ||
Medical condition: Depression, anxiety, sleep disorders | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-007166-37 | Sponsor Protocol Number: TECHUB2007 | Start Date*: 2009-02-04 | |||||||||||
Sponsor Name:MIKEL URRETAVIZCAYA SARACHAGA | |||||||||||||
Full Title: “TERAPIA ELECTROCONVULSIVA DE CONSOLIDACIÓN ASOCIADA A PSICOFÁRMACOS VERSUS FARMACOTERAPIA EN LA PREVENCIÓN DE RECIDIVAS EN EL TRASTORNO DEPRESIVO MAYOR. UN ENSAYO CLÍNICO, PRAGMÁTICO, PROSPECTIVO ... | |||||||||||||
Medical condition: TRASTORNO DEPRESIVO MAYOR | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004478-24 | Sponsor Protocol Number: OV101-18-002 | Start Date*: 2020-06-05 | |||||||||||
Sponsor Name:Ovid Therapeutics Inc. | |||||||||||||
Full Title: An Open-Label Study to Evaluate the Long-Term Safety, Tolerability, and Efficacy of OV101 in Individuals with Angelman Syndrome (ELARA) | |||||||||||||
Medical condition: Angelman Syndrome | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002907-17 | Sponsor Protocol Number: OV101-19-001 | Start Date*: 2020-02-19 | |||||||||||
Sponsor Name:Ovid Therapeutics Inc. | |||||||||||||
Full Title: A MulticeNter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 3 Study to Evaluate the Efficacy and Safety of OV101 in PediaTric IndividUals With AngelmaN SyndromE (NEPTUNE) | |||||||||||||
Medical condition: Angelman Syndrome | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004645-36 | Sponsor Protocol Number: TMP-2501-2019-2 | Start Date*: 2021-05-31 | |||||||||||
Sponsor Name:Fraunhofer Gesellschaft for its Fraunhofer Institute for Translational Medicine and Pharmacology (ITMP) | |||||||||||||
Full Title: Impact of different silymarin dosages to decrease drug-induced elevated liver enzymes compared to placebo in a prospective controlled dose finding Phase IIb trial (SILVER) | |||||||||||||
Medical condition: Drug-induced elevated liver enzymes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003405-22 | Sponsor Protocol Number: CTP3S1502HT6 | Start Date*: 2022-09-02 | |||||||||||
Sponsor Name:Suven Life Sciences Ltd. | |||||||||||||
Full Title: A Phase 3, Double-Blind, Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of Masupirdine (SUVN-502) for the Tre... | |||||||||||||
Medical condition: Agitation with Dementia of the Alzheimer's Type | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) HR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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