- Trials with a EudraCT protocol (475)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
475 result(s) found for: Brain surgery.
Displaying page 1 of 24.
EudraCT Number: 2021-003716-12 | Sponsor Protocol Number: RHNIA-001-2021 | Start Date*: 2022-08-24 | ||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet | ||||||||||||||||||||||||||||
Full Title: S-ketamine for cortical spreading depolarisation in patients with severe acute brain injury | ||||||||||||||||||||||||||||
Medical condition: Severe acute brain injury caused by aneurysmal subarachnoid hemorrhage, spontaneous intracerebral hemorrhage or traumatic brain injury. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006301-10 | Sponsor Protocol Number: MAGNA | Start Date*: 2012-05-10 | ||||||||||||||||
Sponsor Name:Fundació Clinic per a la Recerca Biomèdica | ||||||||||||||||||
Full Title: Perioperative Magnesium Sulphate as a cerebral protector in neurosurgical patients | ||||||||||||||||||
Medical condition: Patient who are going to be under cerebral parenchyma resection, due to epilepsy or tumor | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011696-68 | Sponsor Protocol Number: 09014 | Start Date*: 2009-10-09 | ||||||||||||||||||||||||||
Sponsor Name:University of Nottingham | ||||||||||||||||||||||||||||
Full Title: The effect of drugs used to reverse neuromuscular blockade on intra-cranial pressure | ||||||||||||||||||||||||||||
Medical condition: intracranial pressure changes following craniotomy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-004512-58 | Sponsor Protocol Number: INV-GEM-0200-I | Start Date*: 2020-08-17 | |||||||||||
Sponsor Name:Technische Universität München, Fakultät für Medizin | |||||||||||||
Full Title: Comparison of Fluorescein-INtra-VItal microscopy Versus conventional frozen section diagnosis for intraOperative histopathological evaluation | |||||||||||||
Medical condition: Intracranial tumor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001322-54 | Sponsor Protocol Number: CS/2018/6632 | Start Date*: 2020-06-15 | ||||||||||||||||||||||||||
Sponsor Name:University Hospitals Bristol and Weston NHS Foundation Trust | ||||||||||||||||||||||||||||
Full Title: Carbon Dioxide Insufflation and Brain Protection During Open Heart Surgery: A Randomised Controlled Trial | ||||||||||||||||||||||||||||
Medical condition: Brain injury during open heart valve surgery | ||||||||||||||||||||||||||||
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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: 2008-007349-30 | Sponsor Protocol Number: ML21873 | Start Date*: 2009-04-15 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Open-label, phase II, randomized, comparative, multicentre trial of concurrent Whole Brain Radiation Therapy (WBRT) and capecitabine (Xeloda®) followed by maintenance capecitabine compared with sta... | |||||||||||||
Medical condition: Female breast cancer patients with newly diagnosed CNS metastases with at least one brain lesion measuring ≥0.5 cm in longest dimension, who are not considered candidates for surgery or stereotacti... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023356-90 | Sponsor Protocol Number: 1020 | Start Date*: 2011-01-06 | |||||||||||
Sponsor Name:Oncology Department | |||||||||||||
Full Title: Electrochemotherapy as a palliative treatment for brain metastases | |||||||||||||
Medical condition: Patient with brain metastases from cancer of any histology. A phase I trial. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 2020-003804-15 | Sponsor Protocol Number: SGMCBM | Start Date*: 2023-12-19 | ||||||||||||||||
Sponsor Name:Leiden University Medical Center | ||||||||||||||||||
Full Title: A FEASIBILITY STUDY OF SGM-101, A FLUOROCHROME-LABELED ANTI-CARCINOEMBRYONIC ANTIGEN MONOCLONAL ANTIBODY FOR THE INTRAOPERATIVE DETECTION OF COLORECTAL BRAIN METASTASES | ||||||||||||||||||
Medical condition: Colorectal brain metastases | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007350-35 | Sponsor Protocol Number: ML 22203 | Start Date*: 2009-07-17 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: A single arm, open-label trial assessing the effect of Capecitabine (Xeloda®) on progression-free survival rate at four months in breast cancer patients with CNS progression after whole brain radio... | |||||||||||||
Medical condition: Female breast cancer patients with progression of brain metastasis following WBRT and at least one measurable lesion in the brain (defined as any lesion >1 cm in longest dimension at MRI). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003003-31 | Sponsor Protocol Number: EORTC 26082 – 22081 | Start Date*: 2009-12-01 | |||||||||||
Sponsor Name:EORTC Headquarters | |||||||||||||
Full Title: Radiation therapy and concurrent plus adjuvant Temsirolimus (CCI-779) versus chemo-irradiation with Temozolomide in newly diagnosed glioblastoma without methylation of the MGMT gene promoter – a ra... | |||||||||||||
Medical condition: patients with newly diagnosed glioblastoma (GBM) without methylation of the DNA-repair enzyme O6-methylguanin-DNA-methyltransferase (MGMT) gene promoter | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) NL (Completed) BE (Completed) GB (Completed) AT (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007106-30 | Sponsor Protocol Number: 45938032 | Start Date*: 2008-01-29 | ||||||||||||||||
Sponsor Name:HUS, ATEK, Töölön sairaala, Neurokirurgian klinikka | ||||||||||||||||||
Full Title: Tavoite-ohjattu nestehoito istuvan neurokirurgisen potilaan anestesiassa | ||||||||||||||||||
Medical condition: Neurokirurgisia potilaita. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-000889-36 | Sponsor Protocol Number: H6Q-MC-S020 | Start Date*: 2006-08-10 |
Sponsor Name:Eli Lilly and Company limited | ||
Full Title: A Double-blind, Randomized, Placebo-controlled Multicentre Phase II Study of Maintenance Enzastaurin Following Whole Brain Radiation Therapy in the Treatment of Brain Metastases from Lung Cancer | ||
Medical condition: brain metastastases of non-small or small cell lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) SE (Completed) DK (Completed) PL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-001119-30 | Sponsor Protocol Number: 2B3-101-CR-001 | Start Date*: 2011-06-22 | |||||||||||||||||||||||||||||||
Sponsor Name:to-BBB technologies B.V. | |||||||||||||||||||||||||||||||||
Full Title: An open-label, Phase I/IIa, dose escalating study of 2B3-101 in patients with solid tumors and brain metastases or recurrent malignant glioma. | |||||||||||||||||||||||||||||||||
Medical condition: Solid tumors and brain metastases or recurrent malignant glioma, HER2-positive adenocarcinoma of the breast with brain metastases | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002714-11 | Sponsor Protocol Number: EORTC 22033-26033 | Start Date*: 2005-06-06 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Primary chemotherapy with temozolomide vs. radiotherapy in patients with low grade gliomas after stratification for genetic 1p loss: a phase III study | |||||||||||||
Medical condition: Histologically proven low-grade glioma ♦ Astrocytoma WHO grade II (gemistocytic, fibrillary and protoplasmatic) ♦ Oligoastrocytoma WHO grade II ♦ Oligodendroglioma WHO grade II | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) GB (Completed) IT (Completed) DK (Prematurely Ended) BE (Completed) ES (Completed) PT (Completed) HU (Completed) SE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003916-19 | Sponsor Protocol Number: 001 | Start Date*: 2015-12-30 |
Sponsor Name:Karl Landsteiner Institut für klinische Neurologie und Neuropsycholigie | ||
Full Title: Perioperative Levetiracetam for seizure prophylaxis in brain tumor patients. Prospective evaluation of side effects and efficacy | ||
Medical condition: Data on perioperative seizure prophylaxis in brain tumor patients as weil as on specific side effects is limited in scientific literature. Epileptic seizures during and after brain tumor surgery ma... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
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: 2015-001166-26 | Sponsor Protocol Number: M13-813 | Start Date*: 2015-12-28 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Placebo Controlled Phase 3 Study of ABT-414 with Concurrent Chemoradiation and Adjuvant Temozolomide in Subjects with Newly Diagnosed Glioblastoma (GBM) with Epidermal Growth Factor R... | |||||||||||||
Medical condition: Newly diagnosed glioblastoma (GBM) or gliosarcoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) NL (Completed) IE (Completed) DE (Completed) BE (Completed) AT (Completed) GB (GB - no longer in EU/EEA) PT (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005565-40 | Sponsor Protocol Number: OTP-B-Linköping | Start Date*: 2014-09-11 |
Sponsor Name:Department of Biomedical Engineering, Linköping University | ||
Full Title: Optical measurement with 5-ALA during surgical resection of brain tumors in children | ||
Medical condition: Tumour border by means of fluorescenstechnique during surgical resection of brain tumours. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-006288-36 | Sponsor Protocol Number: 1200.24 | Start Date*: 2009-03-16 | |||||||||||||||||||||
Sponsor Name:Boehringer Ingelheim Limited | |||||||||||||||||||||||
Full Title: Phase II open label trial to assess the efficacy and the impact on QTcF of continuous oral BIBW 2992 at a daily dose of 50 mg in patients with relapsed or refractory solid tumours including patient... | |||||||||||||||||||||||
Medical condition: Patients diagnosed with EGFR/HER2-positive solid tumour cancers with and without brain metastases, and patients with recurrent glioblastoma. | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
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