- Trials with a EudraCT protocol (21)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (8)
21 result(s) found for: AUDIT.
Displaying page 1 of 2.
EudraCT Number: 2016-003343-11 | Sponsor Protocol Number: GLP1ALCOHOL | Start Date*: 2017-04-12 | |||||||||||
Sponsor Name:Psychiatric Centre Copenhagen | |||||||||||||
Full Title: Does Glucagon-like Peptide 1 (GLP-1) receptor stimulation reduce alcohol intake in patients with alcohol dependence? | |||||||||||||
Medical condition: Alcohol dependence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000829-55 | Sponsor Protocol Number: PSILO4ALCO | Start Date*: 2020-12-16 | ||||||||||||||||
Sponsor Name:Psychiatric Centre Copenhagen | ||||||||||||||||||
Full Title: Can a one-off administration of psilocybin reduce alcohol intake in patients with alcohol use disorder? A randomized, double-blinded, placebo-controlled clinical trial. | ||||||||||||||||||
Medical condition: Alcohol Use Disorder | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004684-31 | Sponsor Protocol Number: 2809SELENIUM | Start Date*: 2006-04-20 |
Sponsor Name:Barts and the London NHS Trust | ||
Full Title: Does Selenium Supplementation reduce Oxidative Stress associated with Subarachnoid Haemorrhage? | ||
Medical condition: Patients with spontaneous subarachnoid haemorrhage (non-traumatic) admitted to the Intensive Vare Unit of the Royal London Hospital. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001456-18 | Sponsor Protocol Number: AZIQUINE-ICU-25032020 | Start Date*: 2020-04-09 |
Sponsor Name:Nadační fond Donatio intensivistam | ||
Full Title: Azithromycin added to Hydrochloroquine in Patients Admitted to Intensive Care due to Coronavirus Disease 2019 (COVID-19) - Randomised Controlled Trial, phase III | ||
Medical condition: Severe COVID-19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2023-000224-10 | Sponsor Protocol Number: PBKV.5zdnia03.08.2022 | Start Date*: 2023-08-17 |
Sponsor Name:The Pharmaceutical Company LEK-AM Sp. Zo.o. | ||
Full Title: A randomized, double-blind, placebo-controlled, multicentre study to evaluate the effect of a 12-week dose of 35 mg DHEA on quality of life in menopausal women. | ||
Medical condition: Menopause | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-004160-16 | Sponsor Protocol Number: PBKV.8zdnia01.06.2022 | Start Date*: 2024-02-22 |
Sponsor Name:The Pharmaceutical Company LEK-AM Sp. Zoo. | ||
Full Title: A randomized, double-blind, placebo-controlled, multicenter study evaluating the effect of a 12-week DHEA combination of 20 mg and 2 mg prolonged-release melatonin on sleep quality an... | ||
Medical condition: Menopause, sleep disorders in the postmenopausal period | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: PL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000229-35 | Sponsor Protocol Number: 2015/01 | Start Date*: 2016-11-03 |
Sponsor Name:Beaumont Hospital | ||
Full Title: A prospective randomised control trial comparing local anaesthetic subcutaneous wound injection versus local anaesthetic wound percolation in distal forearm fractures | ||
Medical condition: Fracture of distal radius or ulna | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005248-17 | Sponsor Protocol Number: 1160.71 | Start Date*: 2008-11-20 | |||||||||||
Sponsor Name:Boehringer Ingelheim AB | |||||||||||||
Full Title: RELY-ABLE long term multi-center extension of dabigatran treatment in patients with atrial fibrillation who completed the RE-LY trial and a cluster randomised trial to assess the effect of a knowle... | |||||||||||||
Medical condition: This is a study of the long term safety of dabigatran (intended indication: stroke prevention in patients with atrial fibrillation).Eligible patients received dabigatran during the RE-LY trial 1160... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) NL (Completed) FI (Completed) DE (Completed) DK (Completed) AT (Completed) GB (Completed) SK (Completed) FR (Completed) BE (Completed) HU (Completed) PL (Completed) CZ (Completed) IT (Completed) PT (Completed) BG (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001946-93 | Sponsor Protocol Number: NalGamb | Start Date*: 2017-10-31 | |||||||||||
Sponsor Name:National Instute of Health and Welfare | |||||||||||||
Full Title: Double-blind, placebo-controlled randomised study on the efficacy of naloxone nasal spray for the treatment of gambling disorder | |||||||||||||
Medical condition: Problem gambling | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004988-42 | Sponsor Protocol Number: 12DIAB15 | Start Date*: 2013-02-05 | ||||||||||||||||
Sponsor Name:Sandwell and West Birmingham Hospitals NHS Trust | ||||||||||||||||||
Full Title: REVISE-Diabesity: Randomisation to Endoluminal intestinal liner alone Versus with Incretin analogue in SustainEd Diabesity | ||||||||||||||||||
Medical condition: Combined Type 2 diabetes mellitus and obesity. | ||||||||||||||||||
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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: 2010-022496-66 | Sponsor Protocol Number: UCL/09/0398 | Start Date*: 2011-02-21 | |||||||||||
Sponsor Name:Joint UCLH and UCL Biomedical Research Unit | |||||||||||||
Full Title: An Evaluation of the Tolerability and Feasibility of combining 5-Amino-Levulinic Acid (5-ALA) with Carmustine Wafers (Gliadel) in the Surgical Management of Primary Glioblastoma (GALA-5 Trial) | |||||||||||||
Medical condition: Primary glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000819-67 | Sponsor Protocol Number: MTW_2020_KC01 | Start Date*: 2020-07-28 |
Sponsor Name:Maidstone and Tunbridge Wells NHS Trust | ||
Full Title: SENTINUS: Technical feasibility and diagnostic accuracy of intradermal microbubbles and contrast enhanced ultrasound to identify sentinel lymph node metastases in breast cancer patients following t... | ||
Medical condition: Breast Cancer - Using SonoVue injected intradermally into the breast and contrast enhanced ultrasound to see if the cancer has spread via lymphatic channels to sentinel lymph nodes in the axilla. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004766-40 | Sponsor Protocol Number: 30592 | Start Date*: 2009-04-08 | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: Rapid Intervention with GTN in Hypertensive stroke Trial (RIGHT). Determining the potential of ambulance-based randomised controlled trials in patients with hyperacute stroke; assessment of glycery... | |||||||||||||
Medical condition: Hypertension in acute stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023969-21 | Sponsor Protocol Number: 724 | Start Date*: 2011-10-28 | |||||||||||
Sponsor Name:Gateshead Health NHS Foundation Trust | |||||||||||||
Full Title: Vascular Augmentation of Late-life Unremitted Depression | |||||||||||||
Medical condition: Late-life (aged 50 or over) unremitted vascular depression. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007026-19 | Sponsor Protocol Number: LANTU_L_04211 | Start Date*: 2009-04-24 | |||||||||||
Sponsor Name:Aventis Pharma Ltd trading as sanofi-aventis | |||||||||||||
Full Title: COMPARISON OF A BASAL PLUS ONE INSULIN REGIMEN (INSULIN GLARGINE/INSULIN GLULISINE) WITH A BIPHASIC INSULIN REGIMEN (INSULIN ASPART/INSULIN ASPART PROTAMINE 30/70) IN TYPE 2 DIABETES PATIENTS FOLLO... | |||||||||||||
Medical condition: Type II diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000048-24 | Sponsor Protocol Number: COMB-BO8 | Start Date*: 2018-12-28 |
Sponsor Name:Sahlgrenska University Hospital/VGR | ||
Full Title: A RANDOMIZED DOUBLE-BLIND PLACEBO-CONTROLLED MULTICENTER TRIAL ON THE EFFICACY OF VARENICLINE AND BUPROPION, IN COMBINATION AND ALONE, FOR THE TREATMENT OF ALCOHOL USE DISORDER | ||
Medical condition: Alcohol Use Disorder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001249-11 | Sponsor Protocol Number: Parachutes | Start Date*: 2021-07-14 | |||||||||||
Sponsor Name:Karolinska Universitetssjukhuset | |||||||||||||
Full Title: PARACHUTES: Pedophilia At Risk – Acute Treatment – E-therapy vs SSRI | |||||||||||||
Medical condition: Pedophilic Disorder | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022307-22 | Sponsor Protocol Number: BergenPsychosisProject2 | Start Date*: 2011-04-14 | |||||||||||
Sponsor Name:Haukeland University Hospital, Division of Psychiatry | |||||||||||||
Full Title: The Bergen Psychosis Project 2 | |||||||||||||
Medical condition: Patients with schizophrenia and related non-affective psychotic disorders, corresponding to ICD-10 diagnoses F10.5-19.5, and F20-29. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004740-30 | Sponsor Protocol Number: PHRCN2018 | Start Date*: 2021-09-15 | |||||||||||
Sponsor Name:Centre Hospitalier Le Vinatier | |||||||||||||
Full Title: Cannabidiol for reducing drinking in alcohol use disorder and modifying the effects of alcohol on the brain and the liver: a phase 2 clinical trial. | |||||||||||||
Medical condition: CARAMEL is an exploratory phase-2 study conducted in subjects with AUD (alcohol use disorder) and current heavy drinking level, aiming to confirm the different properties of CBD observed in animal ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004707-38 | Sponsor Protocol Number: CCR 3065 | Start Date*: 2005-04-08 | |||||||||||
Sponsor Name:Royal Marsden NHS Trust | |||||||||||||
Full Title: A multicentre randomised phase II clinical trial comparing oxaliplatin (Eloxatin), capecitabine (Xeloda) and pre-operative radiotherapy with or without cetuximab followed by total mesorectal excisi... | |||||||||||||
Medical condition: High risk operable rectal adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Ongoing) SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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