- Trials with a EudraCT protocol (352)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
352 result(s) found for: Brain development.
Displaying page 1 of 18.
EudraCT Number: 2005-001281-13 | Sponsor Protocol Number: KS-2004-06-SET | Start Date*: 2005-11-15 |
Sponsor Name:DSC Services, s.r.o. | ||
Full Title: Observational Study of Early Interferon beta 1-a Treatment in High Risk Subjects after CIS (SET Study) | ||
Medical condition: Clinically isolated syndrome suspected from demyelinating event (no better explanation for present symptoms) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004596-31 | Sponsor Protocol Number: NL62772 | Start Date*: 2019-03-25 | ||||||||||||||||
Sponsor Name:UMC Utrecht | ||||||||||||||||||
Full Title: CeRebrUm and CardIac protection with Allopurinol in neonates with critical congenital heart disease requiring cardiac surgery with cardiopulmonary bypass | ||||||||||||||||||
Medical condition: Brain injury in neonates with critical congenital heart disease requiring cardiac surgery with cardiopulmonary bypass. | ||||||||||||||||||
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Population Age: Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005912-28 | Sponsor Protocol Number: EGF107671 | Start Date*: 2007-04-16 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd. | |||||||||||||
Full Title: Study EGF107671 – a Phase II Study of Lapatinib plus Topotecan or Lapatinib plus Capecitabine in the Treatment of Recurrent Brain Metastases from ErbB2-Positive Breast Cancer Following Cranial Radi... | |||||||||||||
Medical condition: Brain metastases from ErbB2-positive breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) ES (Completed) BE (Completed) AT (Completed) FR (Completed) GR (Completed) IT (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003099-39 | Sponsor Protocol Number: LWH0604 | Start Date*: 2008-08-21 |
Sponsor Name:Liverpool Women's NHS Foundation Trust Hospital | ||
Full Title: A Randomised Controlled Trial of Thyroxine in Preterm Infants Under 28 weeks' Gestation. | ||
Medical condition: Hypothyroidism is a condition where there is a lack of thyroid hormone in the body. Thyroid hormones are important for normal brain development and growth. Children who are born with low thyroid ho... | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011824-79 | Sponsor Protocol Number: 91686125 | Start Date*: 2009-11-03 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Effects of fluoxetine on the outgrowth of the serotonergic system | |||||||||||||
Medical condition: We investigate whether the effects fluoxetine (Prozac®) on the outgrowth of the serotonergic system are dependent on age. In a 16 week multicenter randomized, double-blind, placebo controlled trial... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000954-46 | Sponsor Protocol Number: MO25743 | Start Date*: 2011-09-26 | |||||||||||
Sponsor Name:F. Hoffman-La Roche Ltd. | |||||||||||||
Full Title: An open-label, single-arm, phase II, multicenter study to evaluate the efficacy of vemurafenib in metastatic melanoma patients with brain metastases | |||||||||||||
Medical condition: Metastatic Melanoma with Brain Metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005647-24 | Sponsor Protocol Number: MIA2019/CT/258 | Start Date*: 2021-05-10 | |||||||||||
Sponsor Name:Melanoma Institute Australia | |||||||||||||
Full Title: A phase II, open label, randomised trial of ipilimumab and nivolumab with concurrent intracranial stereotactic radiotherapy versus ipilimumab and nivolumab alone in patients with melanoma brain met... | |||||||||||||
Medical condition: melanoma brain metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Prematurely Ended) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002074-22 | Sponsor Protocol Number: UM2005/00201/00 | Start Date*: 2006-10-18 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A Randomized, Phase III, Open-Label Study of Oral Topotecan Plus Whole-Brain Radiation Therapy (WBRT) Compared with WBRT Alone in Patients with Brain Metastases from Non-Small Cell Lung Cancer. | ||
Medical condition: Brain metastases from primary non-small cell lung cancer (NSCLC). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001466-42 | Sponsor Protocol Number: 17-HPNCL-02 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Fondation Lenval - Hôpitaux Pédiatriques de Nice CHULENVAL | |||||||||||||
Full Title: EFFECTIVENESS OF INTRANASAL DEXMEDETOMIDINE FOR SEDATED AUDITORY BRAINSTEM RESPONSE TESTING | |||||||||||||
Medical condition: Child requiring auditory evaluation in a context of suspicion of deafness, language delay, overall developmental delay, risk factors for hearing loss. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003190-26 | Sponsor Protocol Number: RESTART13 | Start Date*: 2013-01-14 | |||||||||||
Sponsor Name:ACCORD (Academic and Clinical Central Office for Research & Development) [...] | |||||||||||||
Full Title: REstart or STop Antithrombotics Randomised Trial (RESTART) | |||||||||||||
Medical condition: Spontaneous Intracerebral Haemorrhage (ICH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005044-86 | Sponsor Protocol Number: flu2006 | Start Date*: 2007-02-07 | |||||||||||
Sponsor Name:Roessingh Research and Development | |||||||||||||
Full Title: Influence of long-term administration of fluoxetine on cerebral threshold and muscle activity patterns in chronic stroke patients. | |||||||||||||
Medical condition: The effect of fluoxetine on brain excitability and muscle activation will be measured in chronic stroke patients (> 6 months after stroke). As secondary measures, also brain activation, phase-synch... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005319-66 | Sponsor Protocol Number: 2005/W/AN/02 | Start Date*: 2006-06-02 |
Sponsor Name:Research and Development Office, Royal Infirmary of Edinburgh | ||
Full Title: A comparative study of HyperHAES (7.2% NACL and 6% hydroxyethyl starch) and 20% mannitol in the treatment of elevated intracranial pressure after brain injry | ||
Medical condition: elevated intracranial pressure after brain injury | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001491-21 | Sponsor Protocol Number: 1-2006 | Start Date*: Information not available in EudraCT |
Sponsor Name:Max Planck Institute of Psychiatry | ||
Full Title: Studies on Permeability of the Blood-Brain-Barrier for Escitaloprame related to various Genotypes of the ABCB1-Gene: Effects on Sleep and Motoric Learning | ||
Medical condition: Effects on sleep electroencephalogram and motoric learning in healthy volunteers related to the permeability of the blood-brain-barrier related to genotypes of the ABCB 1 gene | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001912-20 | Sponsor Protocol Number: 48431 | Start Date*: 2018-02-26 |
Sponsor Name:University Medical Center Utrecht, The Netherlands | ||
Full Title: Adult mesenchymal stem cells to regenerate the neonatal brain: the PASSIoN trial (Perinatal Arterial Stroke treated with Stem cells IntraNasally) | ||
Medical condition: Perinatal arterial Ischemic Stroke (PAIS) | ||
Disease: | ||
Population Age: Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001688-66 | Sponsor Protocol Number: SC.14/18-19 | Start Date*: 2019-09-09 | |||||||||||
Sponsor Name:University of Warwick [...] | |||||||||||||
Full Title: Sugar or Salt (SOS) trial: Hyperosmolar therapy in traumatic brain injury | |||||||||||||
Medical condition: Increased intracranial pressure following traumatic brain injury | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003199-56 | Sponsor Protocol Number: CA209-322 | Start Date*: 2016-01-08 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: An open-label, single-arm, phase II, multicenter study to evaluate the efficacy of nivolumab/ipilimumab combination therapy in metastatic melanoma patients with symptomatic brain metastases. | ||
Medical condition: Metastatic (stage IV) melanoma with symptomatic brain metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023654-37 | Sponsor Protocol Number: 34509 | Start Date*: 2011-03-24 | ||||||||||||||||
Sponsor Name:Academic Medical Center | ||||||||||||||||||
Full Title: Effects of methylphenidate on the development of the dopaminergic system in the brain | ||||||||||||||||||
Medical condition: This project investigates whether the effects of methylfenidate on the outgrowth of the dopaminergic system are dependent on age. In a 16 week multicenter, dounle-blind, placebo controlled trial wi... | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003722-25 | Sponsor Protocol Number: U1111-1201-0087 | Start Date*: 2020-12-14 | |||||||||||
Sponsor Name:University of Cincinnati | |||||||||||||
Full Title: rFVIIa for Acute Hemorrhagic Stroke Administered at Earliest Time (FASTEST) Trial | |||||||||||||
Medical condition: Acute haemorrhagic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000612-34 | Sponsor Protocol Number: EpoRepair | Start Date*: 2015-12-15 |
Sponsor Name:UniversitätsSpital Zürich | ||
Full Title: Erythropoietin for the repair of cerebral injury in very preterm infants, a randomized, double-blind, placebo-controlled, prospective, and multicenter clinical study | ||
Medical condition: 1 out of 100 children born extremely early, or more than 8 weeks before the expected date. 20% of these extremely preterm children shows a cerebral hemorrhage at birth, leading to a significantly i... | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004325-16 | Sponsor Protocol Number: RC31/16/8407 | Start Date*: 2016-12-22 |
Sponsor Name:University Hospital of Toulouse | ||
Full Title: Long term evaluation of infants aged from 3 to 4 years old included in the OTBB2 study (repeated administrations of oxytocin in infants with PWS aged from 0 to 6 months) and comparison with not tre... | ||
Medical condition: Prader Willi Syndrom | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
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