- Trials with a EudraCT protocol (47)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
47 result(s) found for: Psychological development.
Displaying page 1 of 3.
EudraCT Number: 2011-005717-36 | Sponsor Protocol Number: 1645-CI-057 | Start Date*: 2012-06-14 |
Sponsor Name:Instituto de Investigación Sanitaria La Fe | ||
Full Title: Extremely low gestational age neonates randomly an assigned to be blindly resuscitated with 21% vs. 60% oxygen: influence upon mortality and chronic conditions in the neonatal period. | ||
Medical condition: Preterm infants aged 30 weeks or less, who need resuscitation / stabilization maneuvers with positive pressure ventilation immediately after birth | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000156-11 | Sponsor Protocol Number: S65914 | Start Date*: 2022-02-25 |
Sponsor Name:KU Leuven | ||
Full Title: Oxytocin and the development of attachment: Looking beyond the expected? | ||
Medical condition: General healthy population children (ages 8 - 13 years old). | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002196-35 | Sponsor Protocol Number: 73520 | Start Date*: 2020-11-16 |
Sponsor Name:Amsterdam UMC, location VUmc | ||
Full Title: post-trial access cohort BUmetanide for Developmental DIsorders | ||
Medical condition: Neurodevelopmental disorders Autism spectrum disorder Attention deficit hyperactivity disorder (ADHD) Learning disorders | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000396-14 | Sponsor Protocol Number: 3/006/11 | Start Date*: 2011-06-15 | |||||||||||||||||||||
Sponsor Name:University of Aberdeen [...] | |||||||||||||||||||||||
Full Title: The use of Ketamine as an anaesthetic during electroconvulsive therapy (ECT) for depression: does it improve treatment outcome? | |||||||||||||||||||||||
Medical condition: Depression. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002477-59 | Sponsor Protocol Number: CDGP1 | Start Date*: 2012-12-12 | |||||||||||
Sponsor Name:Taneli Raivio, Helsingin yliopistollinen keskussairaala | |||||||||||||
Full Title: Constitutional Delay of Growth and Puberty: towards evidence-based treatment | |||||||||||||
Medical condition: constitutional delay of puberty | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000955-40 | Sponsor Protocol Number: CI-1008-152 | Start Date*: 2004-09-23 |
Sponsor Name:Pfizer Global Research & Development | ||
Full Title: A Placebo-Controlled Study of Pregabalin in Elderly Patients With Generalized Anxiety Disorder | ||
Medical condition: Generalized Anxiety Disorder | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: LV (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002010-35 | Sponsor Protocol Number: TinnEx | Start Date*: 2006-12-14 |
Sponsor Name:Prof. Herta Flor, Head of the Institute of Clinical and Cognitive Neuroscience | ||
Full Title: An Extinction Training in Tinnitus | ||
Medical condition: The effect of pregabalin on the success to reduce the interference by tinnitus by an extinction training is tested in chronic tinnitus sufferers. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002177-35 | Sponsor Protocol Number: GNB-2015 | Start Date*: 2018-05-07 |
Sponsor Name:Masarykova univerzita | ||
Full Title: The effect of gabapentin used as a preemptive to the emergence and development chronic neuropathic pain in patients after spinal cord trauma | ||
Medical condition: Chronic neuropathic pain in patients after spinal cord trauma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003231-19 | Sponsor Protocol Number: ViRap | Start Date*: Information not available in EudraCT |
Sponsor Name:The Children's Memorial Health Institute | ||
Full Title: Randomized, placebo-controlled, double-blind and double-dummy clinical trial comparing the safety, tolerability, and efficacy of vigabatrin and rapamycin in a preventive treatment of infants with T... | ||
Medical condition: Tuberous Sclerosis Complex Epilepsy Tumors associated with Tuberous Sclerosis Complex | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: PL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000643-25 | Sponsor Protocol Number: 205520003 | Start Date*: 2011-04-19 | ||||||||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | ||||||||||||||||||
Full Title: The Qure study: Q-fever fatigue syndrome - response to treatment | ||||||||||||||||||
Medical condition: Q fever fatigue syndrome (QFS) is one of the most frequent sequelae of Q fever. QFS leads to substantial morbidity, a high socio-economic burden and an increased use of healthcare facilities. QFS: ... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-001877-13 | Sponsor Protocol Number: TMT107235 | Start Date*: 2006-08-24 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A randomised, double-blind, double-dummy, parallel-group, placebo-controlled study comparing correlates of brain functional activation before and after treatment with placebo, active comparator par... | ||
Medical condition: Major Depressive Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-001244-38 | Sponsor Protocol Number: 14SM1971 | Start Date*: 2014-07-16 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Preventing Recurrent Gestational Diabetes Mellitus with Early Metformin Intervention | |||||||||||||
Medical condition: Gestational diabetes mellitus. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002726-84 | Sponsor Protocol Number: SHP607-203 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Premacure AB | |||||||||||||
Full Title: Long-Term Safety and Efficacy Outcomes Following Previously Administered Short-Term Treatment with SHP607 in Extremely Premature Infants | |||||||||||||
Medical condition: Chronic Lung Disease | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000961-10 | Sponsor Protocol Number: NITRO Protocol | Start Date*: 2011-12-07 | |||||||||||
Sponsor Name:Royal Liverpool and Broadgreen University Hospitals Trust | |||||||||||||
Full Title: Neoadjuvant IntraviTreal Ranibizumab treatment in high risk Ocular melanoma patients: A two stage single centre Phase II single arm study (NITRO Trial) | |||||||||||||
Medical condition: Uveal Melanoma (requiring enucleation) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002976-14 | Sponsor Protocol Number: CRI103143 | Start Date*: 2006-09-27 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: A phase IIa, single-centre, randomised, placebo-controlled, double-blind, three-period crossover exploratory study investigating the effects on gut autonomic responses of single administrations of ... | ||
Medical condition: Irritable Bowel Syndrome (IBS) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002995-13 | Sponsor Protocol Number: S28720 UZ KUL | Start Date*: 2006-01-23 |
Sponsor Name:UZLeuven | ||
Full Title: An open label Phase II trial to investigate the cardiac effects of pegylated liposomal doxorubicine (Caelyx) in elderly breast cancer patients with new imaging and biochemical techniques. | ||
Medical condition: histologically proven early breast cancer requiring adjuvant chemotherapy according to the treating physician (lymph node positive or other features of high risk according to St-Gallen criteria). 1... | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004959-36 | Sponsor Protocol Number: 446002504 | Start Date*: 2020-09-30 |
Sponsor Name:ZonMw | ||
Full Title: A proof of concept phase II study with the PDE-4 inhibitor roflumilast in patients with mild cognitive impairment (MCI). | ||
Medical condition: Mild Cognitive Impairment (MCI) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002392-28 | Sponsor Protocol Number: RM-493-Supplementation-Therapy | Start Date*: 2014-11-28 |
Sponsor Name:Charité Univeritaetsmedizin Berlin | ||
Full Title: Setmelanotide (RM-493) Treatment Trial in Patients with rare genetic disorders of obesity | ||
Medical condition: Body weight is regulated within the hypothalamus. In rare cases mutations in genes, which are embedded in the signaling cascades of the hypothalamus lead to early onset severe obesity. POMC is one ... | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001542-17 | Sponsor Protocol Number: T109/2019Xe-SAH | Start Date*: 2020-09-17 | |||||||||||
Sponsor Name:Timo Laitio | |||||||||||||
Full Title: Effect of xenon on brain injury, neurological outcome and survival in patients after aneurysmal subarachnoid hemorrhage | |||||||||||||
Medical condition: Acute rupture of cerebral aneurysm, subarachnoid hemorrhage (SAH), unconsciousness, brain injury. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003841-86 | Sponsor Protocol Number: Y-52-52120-214 | Start Date*: 2015-04-30 | |||||||||||
Sponsor Name:Ipsen Innovation | |||||||||||||
Full Title: A phase III, randomised, double blind, placebo controlled and open label phase, multicentre study to investigate the efficacy and safety of BTX-A-HAC NG in the treatment of moderate to severe glabe... | |||||||||||||
Medical condition: Moderate to severe Glabellar lines | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
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