Derniers essais


EudraCT Number: 2006-003934-14 Sponsor Protocol Number: 86,1,2006_06_01 Start Date:
Sponsor Name: Universitätsmedizin Göttingen
Full Title: „Eine randomisierte, placebokontrollierte Doppelblindstudie zur Evaluation der Effektivität oral verabreichten Doxycyclins bei Patienten mit Creutzfeldt-Jakob-Krankheit“
Medical condition: Creutzfeldt-Jakob-Krankheit
Disease: Version SOC Term Classification Code Term Level
14.0 10021881 - Infections and infestations 10055172 Creutzfeld-Jakob disease LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: (No results available)

EudraCT Number: 2004-004443-22 Sponsor Protocol Number: Spirig I 04-05 Start Date:
Sponsor Name: Spirig Pharma AG
Full Title: Untersuchung der Wirksamkeit einer glycerinhaltigen Creme bei der Behandlung von Atopischer Dermatitis. Kontrolliert, randomisierte Doppel-Blind-Studie.
Medical condition: Atopic Dermatitis
Disease: Version SOC Term Classification Code Term Level
7.0 10012438
Population Age: Adolescents, Under 18, Adults Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: (No results available)
EudraCT Number: 2017-001550-34 Sponsor Protocol Number: TIGEM2-PDH Start Date:
Sponsor Name: FONDAZIONE TELETHON
Full Title: Studio clinico pilota per valutare l’efficacia della terapia con fenilbutirrato in pazienti affetti da deficit di piruvato deidrogenasi
Medical condition: La Sperimentazione verrà eseguita su pazienti affetti da difetto dell’enzima piruvato deidrogenasi.I pazienti affetti da questa malattia manifestano aumento dei livelli di lattato nel sangue e nell...
Disease: Version SOC Term Classification Code Term Level
20.0 10027433 - Metabolism and nutrition disorders 10058097 Metabolic disorder PT
20.1 10027433 - Metabolism and nutrition disorders 10000491 Acidosis lactic LLT
20.0 10022891 - Investigations 10037677 Pyruvate LLT
20.0 10022891 - Investigations 10023660 Lactate increased LLT
20.0 10022891 - Investigations 10057975 Lactate pyruvate ratio PT
Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: IT (Ongoing)
Trial results: (No results available)

EudraCT Number: 2018-003199-10 Sponsor Protocol Number: OLE-NLRC4/XIAP.2016.001 Start Date:
Sponsor Name: AB2 Bio Ltd.
Full Title: Open-label extension study with Tadekinig alfa (r-hIL-18BP) to monitor safety and tolerability in patients with IL-18 driven monogenic autoinflammatory conditions: NLRC4 mutation and XIAP deficiency
Medical condition: NLRC4 mutation XIAP deficiency
Disease: Version SOC Term Classification Code Term Level
Population Age: Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: DE (Ongoing)
Trial results: (No results available)
EudraCT Number: 2012-000856-33 Sponsor Protocol Number: 2012-40 Start Date:
Sponsor Name: Institut Pasteur
Full Title: A phase I/II, open-label, study of intracerebral administration of adeno-associated viral vector containing the human alpha-N-acetylglucosaminidase cDNA in children with Sanfilippo type B syndrome
Medical condition: Mucopolysaccharidosis III B
Disease: Version SOC Term Classification Code Term Level
17.0 10010331 - Congenital, familial and genetic disorders 10056890 Mucopolysaccharidosis III PT
Population Age: Infants and toddlers, Children, Under 18 Gender: Male, Female
Trial protocol: FR (Completed)
Trial results: View results

EudraCT Number: 2010-021474-11 Sponsor Protocol Number: GE-001-013 Start Date:
Sponsor Name: GE Healthcare Ltd. and its Affiliates
Full Title: A Multicentre, Randomised, Open-label, Comparative Phase IV Trial To Assess Changes in Dementia Diagnostic Category and Diagnostic Confidence After DaTSCAN Imaging in Subjects with an Uncertain Dia...
Medical condition: Subjects with possible Dementia with Lewy Bodies (DLB) who may or may not also fulfil the criteria for Alzheimers Disease (AD)
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed) ES (Ongoing) IT (Completed)
Trial results: View results
EudraCT Number: 2004-001653-28 Sponsor Protocol Number: 03/314 Start Date:
Sponsor Name: The Leeds teaching Hospitals NHS trust
Full Title: A comparison of the effects on prostaglandin synthesis and cytokine production of an olive-oil based lipid emulsion (Clinoloeic) with a soya based emulsion (Intralipid) in newborn infnats receiving...
Medical condition: Prematurity Parenteral nutrition
Disease: Version SOC Term Classification Code Term Level
Population Age: Preterm newborn infants, Newborns, Under 18 Gender: Male, Female
Trial protocol: GB (GB - no longer in EU/EEA)
Trial results: (No results available)

EudraCT Number: 2009-009278-29 Sponsor Protocol Number: S51477 Start Date:
Sponsor Name: UZ Leuven
Full Title: Follow-up studie: Metformin therapie bij kinderen en adolescenten met neurogene of neuromusculaire aandoeningen
Medical condition: Neuromuscular and neurological diseases, associated with obesity and insulin resistance
Disease: Version SOC Term Classification Code Term Level
9.1 10022489 Insulin resistance LLT
9.1 10022489 Insulin resistance PT
9.1 10029883 Obesity LLT
9.1 10065941 Central obesity PT
Population Age: Adolescents, Under 18 Gender: Male, Female
Trial protocol: BE (Ongoing)
Trial results: (No results available)
EudraCT Number: 2009-013956-62 Sponsor Protocol Number: DEMIJO Start Date:
Sponsor Name: University Medical Center of the University Ulm
Full Title: Preparation of Neuroplant® 300mg N in film-coated tablets (St. John´s wort, SJW) in the treatment of mild to moderate Major Depressive Disorder (MDD) in adolescents from 12 to 17 years (inclusive):...
Medical condition: Mild to moderate MDD acc. DSM-IV-TR in adolescents (12−17years inclusive)
Disease: Version SOC Term Classification Code Term Level
12.0 10025453 Major depressive disorder NOS LLT
Population Age: Adolescents, Under 18 Gender: Male, Female
Trial protocol: DE (Prematurely Ended)
Trial results: (No results available)

EudraCT Number: 2009-013499-29 Sponsor Protocol Number: SUNDRO20 Start Date:
Sponsor Name: Technische Universität München
Full Title: Dosisfindungsstudie für Sugammadex und Neostigmin zur Reversierung einer geringen neuromuskulären Restblockade (train of four ratio 0,2) [Sugammadex and Neostigmine dose finding study for reversal ...
Medical condition: Dose finding study for sugammadex and/or neostigmine at residual neuromuscular blockade (whereas residual neuromuscular blockade is defined as a TOF of 0.2 in this study).
Disease: Version SOC Term Classification Code Term Level
9.1 10057286 Neuromuscular blockade reversal LLT
9.1 10057286 Neuromuscular blockade reversal PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: View results
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