- Trials with a EudraCT protocol (93)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
93 result(s) found for: Physical abuse.
Displaying page 1 of 5.
EudraCT Number: 2016-000207-90 | Sponsor Protocol Number: P15-14/BF2.649 | Start Date*: 2016-11-24 | |||||||||||
Sponsor Name:BIPROJET PHARMA | |||||||||||||
Full Title: A Multisite Randomized, Double-Blind, Placebo-Controlled Trial Evaluating Pitolisant (BF2.649) For Alcohol Use Disorder Treatment. | |||||||||||||
Medical condition: Patients with moderate to severe alcohol use disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004823-66 | Sponsor Protocol Number: ELTCAN1 | Start Date*: 2019-04-17 | |||||||||||
Sponsor Name:Radboudumc | |||||||||||||
Full Title: Early-life stress, the endocannabinoid system, and fear memory extinction | |||||||||||||
Medical condition: healthy volunteers | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002369-14 | Sponsor Protocol Number: CHUB-Psy-PAThforsAUD | Start Date*: 2023-07-20 | |||||||||||
Sponsor Name:CHU Brugmann | |||||||||||||
Full Title: Psilocybin-Assisted Therapy for Severe Alcohol Use Disorder: Feasibility, Clinical Efficacy & (Neuro)cognitive Mechanisms. | |||||||||||||
Medical condition: Severe Alcohol Use Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000240-82 | Sponsor Protocol Number: P04279 | Start Date*: 2005-05-05 |
Sponsor Name:AESCA Pharma GesmbH | ||
Full Title: Randomized, controlled Study of Methadone and Buprenrphine in Hepatitis C patients in need of treatment | ||
Medical condition: hepatitis C patients with a history of intravenous drug abuse, who are willing to undergo methadone or buprenorphine substitution | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002315-92 | Sponsor Protocol Number: 12013A | Start Date*: 2008-11-12 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: A 52-week, randomised, double-blind, placebo-controlled, parallel-group, safety, tolerability and efficacy study of nalmefene, as needed use, in patients with alcohol dependence | |||||||||||||
Medical condition: Alcohol dependence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SK (Completed) EE (Completed) GB (Completed) LV (Completed) HU (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002097-38 | Sponsor Protocol Number: ABR62020 | Start Date*: 2018-06-05 |
Sponsor Name:University Medical Centre Utrecht | ||
Full Title: SAMe as an epigenetic treatment of depression in people with childhood trauma, a double blind placebo-controlled trial | ||
Medical condition: Depressive episode in people with childhood trauma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000069-57 | Sponsor Protocol Number: P15-01 | Start Date*: 2017-07-21 | |||||||||||
Sponsor Name:BIOPROJET PHARMA | |||||||||||||
Full Title: A Multisite Randomized Clinical Trial Evaluating BP1.3656 Versus Placebo For Alcohol Use Disorder Treatment | |||||||||||||
Medical condition: Male or female with moderate or severe DSM-5 alcohol use disorder (based on the alcohol use disorders section of MINI) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001154-98 | Sponsor Protocol Number: 15660A | Start Date*: 2013-10-14 | |||||||||||
Sponsor Name:H Lundbeck A/S [...] | |||||||||||||
Full Title: Interventional, randomized, double-blind, cross-over, placebo-controlled study to investigate the effects of nalmefene after single dose on the blood oxygen level dependent (BOLD) fMRI signal in th... | |||||||||||||
Medical condition: Nalmefene (Selincro) is indicated for the reduction of alcohol consumption in adults with alcohol dependence who have a high drinking risk level, without physical withdrawal symptoms and who do not... | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000712-30 | Sponsor Protocol Number: ABR-71432 | Start Date*: 2021-06-07 | |||||||||||
Sponsor Name:Radboudumc | |||||||||||||
Full Title: Targeted glucocorticoid administration to improve safety learning in PTSD patients with HPA axis dysregulation | |||||||||||||
Medical condition: Posttraumatic Stress Disorder (PTSD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002462-32 | Sponsor Protocol Number: SHW01 | Start Date*: 2022-12-09 | |||||||||||
Sponsor Name:Suchthilfe Wien gGmbH | |||||||||||||
Full Title: Pilot study on the safety and feasibility of intravenous opioid agonist therapy (OAT) with Hydagelan® (hydromorphone hydrochloride) in Vienna. | |||||||||||||
Medical condition: Opioid dependence: Opioid dependence is a serious and usually chronic disease that requires treatment, encompasses various psychological and physical dimensions, and is associated with concomitant ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005044-40 | Sponsor Protocol Number: PPL-1021 | Start Date*: 2006-01-26 |
Sponsor Name:Aerovance, Inc | ||
Full Title: A Phase 2a Study To Investigate The Effects Of AER 002 On Mucociliary Clearance In Subjects With Chronic Obstructive Pulmonary Disease (COPD) | ||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002147-27 | Sponsor Protocol Number: | Start Date*: 2005-05-26 |
Sponsor Name:Department of General Psychiatry | ||
Full Title: Influence of treatment of olanzapine and ziprasidone on transcapillary glucose transport in human skeletal muscle | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002871-32 | Sponsor Protocol Number: Rifabupre | Start Date*: 2012-08-28 |
Sponsor Name:Turku University hospital | ||
Full Title: Effects of rifampicin on the pharmacokinetics and pharmacodynamics of sublingual and intravenous buprenorphine: A four-phase cross-over study in healthy subjects. | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000575-14 | Sponsor Protocol Number: SMO032/10/03 | Start Date*: 2012-05-09 | |||||||||||
Sponsor Name:D&A PHARMA | |||||||||||||
Full Title: Randomized, multicenter, double-blind, placebo-controlled study of the safety and efficacy of 4 dose regimens of SMO.IR, an oral solid formulation of sodium oxybate, in the maintenance of alcohol a... | |||||||||||||
Medical condition: maintenance of alcohol abstinence in recently abstinent alcohol-dependent patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) AT (Completed) IT (Completed) SK (Completed) DE (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002836-25 | Sponsor Protocol Number: QGUY/2004/IL 4-13/01 | Start Date*: 2004-12-15 |
Sponsor Name:Aerovance Inc. | ||
Full Title: A Phase IIa Study To Investigate The Effects of AER 001on Antigen Challenge In Atopic Asthmatic Subjects Following Repeated Administration. | ||
Medical condition: Asthma is characterised by an infiltration of the bronchial mucosa with activated T-lymphocytes (T-cells), eosinophils, and to a lessor extent polymorphonuclear leukocytes. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001174-25 | Sponsor Protocol Number: NC501/SC01904 | Start Date*: Information not available in EudraCT |
Sponsor Name:Neurocure Ltd | ||
Full Title: A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO DETERMINE THE EFFICACY, SAFETY AND TOLERABILITY OF A COMBINATION OF GALANTAMINE (AN ACETYLCHOLINESTERASE INHIBITOR) PLUS TRIMIPRAMINE IN SMOKING CESSATION | ||
Medical condition: Healthy subjects who are smokers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-010334-21 | Sponsor Protocol Number: Flu002 | Start Date*: 2009-04-17 |
Sponsor Name:Oxford University | ||
Full Title: A phase IIa study to assess the safety and efficacy of a new influenza vaccine candidate MVA-NP+M1 in healthy adults. | ||
Medical condition: Influenza | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-002077-76 | Sponsor Protocol Number: QGUY/2005/AER 001/-02 | Start Date*: 2005-06-13 |
Sponsor Name:Aerovance Inc | ||
Full Title: A Phase 2a Study To Investigate The Effects of Repeated Administration of AeroDerm in subjects with Atopic Eczema. | ||
Medical condition: Atopic Eczema: a chronic inflammatory pruritic skin disease that follows a relapsing course and is often associated with elevated serum immunoglobulin E (IgE) levels and a personal or family histor... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018900-10 | Sponsor Protocol Number: FLIP110 | Start Date*: 2010-05-11 | |||||||||||
Sponsor Name:Laboratoires Mayoly Spindler | |||||||||||||
Full Title: Safety and preliminary clinical activity of Yarrowia lipolytica lipase (MS1819) in patients with malabsorption syndrome due to exocrine pancreatic insufficiency resulting from chronic pancreatitis | |||||||||||||
Medical condition: Exocrine pancreatic insufficiency resulting from chronic pancreatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000107-36 | Sponsor Protocol Number: VER-CLBP-001 | Start Date*: 2021-03-24 |
Sponsor Name:Vertanical GmbH | ||
Full Title: Proof of efficacy, maintenance of efficacy, long-term safety and investigation of the potential for dependence and abuse and the effect of abrupt drug withdrawal of VER-01 in a multicenter study in... | ||
Medical condition: For the treatment of patients with chronic non-specific low back pain when drug treatment is indicated and previous optimised treatments with non-opioid analgesics have not led to sufficient pain r... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) AT (Completed) | ||
Trial results: (No results available) |
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