- Trials with a EudraCT protocol (18)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
18 result(s) found for: Gamma camera.
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EudraCT Number: 2015-001211-13 | Sponsor Protocol Number: PRODROMALAD | Start Date*: 2015-11-03 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: IMAGING OF NEUROINFLAMMATION AND NEURODEGENERATION IN ALZHEIMER’S DISEASE | |||||||||||||
Medical condition: mild cognitive impairment and familiar Alzheimer disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023120-24 | Sponsor Protocol Number: Nitro1 | Start Date*: 2011-10-18 | |||||||||||
Sponsor Name:MAASTRO clinic | |||||||||||||
Full Title: Nitroglycerin's effect on perfusion and hypoxia in human non small cell lung cancer: proof of principle, a phase II trial | |||||||||||||
Medical condition: non small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003669-24 | Sponsor Protocol Number: NET-2011-02346784 | Start Date*: 2017-01-30 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: Amyloid PET imaging study for the diagnosis of Alzheimer's disease in the preclinical/predementia phase | |||||||||||||
Medical condition: memory complaint, mild cognitive impairment, Alzheimer's Disease in predrmentia/prodromal disease phases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004244-35 | Sponsor Protocol Number: 1/25-03-2014 | Start Date*: 2015-03-05 | |||||||||||
Sponsor Name:IRCCS Ospedale San Raffaele | |||||||||||||
Full Title: AMYLOID LOAD IN PRODROMAL AD WITH LIMBIC-PREDOMINANT PHENOTYPE PRINCIPAL INVESTIGATOR - STUDIO DEL CARICO DI AMILOIDE IN AD PRODROMICO CON FENOTIPO LIMBICO | |||||||||||||
Medical condition: mild cognitive impairment, Alzheimer's disease prodromal | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000959-33 | Sponsor Protocol Number: CTP G007.04 | Start Date*: 2007-08-16 |
Sponsor Name:PARI GmbH | ||
Full Title: Randomized, open labelled, cross over deposition study of Tobramycin 100 PARI nebulized with eFlow® versus TOBI® nebulized with PARI LC PLUS® in subjects with CF | ||
Medical condition: Cystic Fibrosis with Pseudomonas aeruginosa infection | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005389-31 | Sponsor Protocol Number: FBB-HUG-2014 | Start Date*: 2015-02-18 | |||||||||||
Sponsor Name:HôPITAUX UNIVERSITAIRES DE GENèVE | |||||||||||||
Full Title: Incremental diagnostic value of Florbetaben Imaging vs other core biomarkers for Alzheimer Disease in patients with Mild Cognitive Impairment. An Investigator-Initiated Sponsored Study. | |||||||||||||
Medical condition: Mild Cognitive Impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004415-24 | Sponsor Protocol Number: 09/2011MolecularImaging | Start Date*: 2012-01-16 | |||||||||||
Sponsor Name:IRCCS CENTRO SAN GIOVANNI DI DIO | |||||||||||||
Full Title: Molecular imaging for the early diagnosis and monitoring of Alzheimer’s disease in old individuals with cognitive disturbances: an ADNI-compatible prospective study | |||||||||||||
Medical condition: Mild Congitive Impairment (MCI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004328-40 | Sponsor Protocol Number: INMINDFP7-HEALTH-2011-two-stage | Start Date*: 2013-03-01 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE DI MILANO | |||||||||||||
Full Title: IMAGING OF NEUROINFLAMMATION IN NEURODEGENERATIVE DISEASES | |||||||||||||
Medical condition: mild cognitive impairment, Alzheimer disease,frontotemporal dementia, SLA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003268-19 | Sponsor Protocol Number: BR-TUM-ICG-IV-2 | Start Date*: 2014-10-06 |
Sponsor Name:Jules Bordet Institute | ||
Full Title: Study evaluating breast cancer tumorectomy guided by Near-Infrared imaging after the intravenous injection of free Indocyanine Green | ||
Medical condition: Imaging of tumours and their margins after intravenous injection of Indocyanine Green to breast cancer patients | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000267-17 | Sponsor Protocol Number: VPI-103-01 | Start Date*: 2007-02-21 | |||||||||||
Sponsor Name:Verus Pharmaceuticals Inc | |||||||||||||
Full Title: A SINGLE CENTRE, GAMMA SCINTIGRAPHY STUDY IN ASTHMATIC PATIENTS TO COMPARE PULMONARY DEPOSITION AND PHARMACOKINETICS OF ALBUTEROL INHALATION SOLUTION (AIS) DELIVERED VIA eFLOW NEBULISER AND SALBUTA... | |||||||||||||
Medical condition: The medical condition which is under investigation is Asthma. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005546-42 | Sponsor Protocol Number: MELISA | Start Date*: 2021-06-21 | |||||||||||
Sponsor Name:Fundacio Clinic per a la Recerca Biomedica | |||||||||||||
Full Title: Sentinel lymph node assessment in ovarian cancer. Lymphatic mapping with two tracers and intraoperative lymphoscintigraphy. | |||||||||||||
Medical condition: Sentinel lymph node in ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007965-22 | Sponsor Protocol Number: IWT-TBM 0707181 | Start Date*: 2009-06-04 |
Sponsor Name:Nuclear Medicine UZ Gasthuisberg [...] | ||
Full Title: Evaluating diagnostic challenges in the management of neuroendocrine tumours with peptide receptor radionuclide therapy | ||
Medical condition: Patients with a histological proven neuroendocrine tumour, without other curative options. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-003068-28 | Sponsor Protocol Number: 77946 | Start Date*: 2021-09-29 | |||||||||||||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||||||||||||
Full Title: Sentinel lymph node detection of cervical occult lymph node metastases in patients with parotid gland carcinoma by means of sentinel node biopsy using 68-galium-tilmanocept PET-CT. | |||||||||||||||||||||||
Medical condition: The IMP will be used for the identification of sentinel lymph node(s) in patients with parotid gland carcinoma. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003683-12 | Sponsor Protocol Number: SENTOV | Start Date*: 2018-01-23 | |||||||||||
Sponsor Name:INSTITUTO DE INVESTIGACIÓN SANITARIA LA FE | |||||||||||||
Full Title: Sentinel node in ovarian cáncer: tailoring clinical feasibility | |||||||||||||
Medical condition: Early stage ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002341-35 | Sponsor Protocol Number: GA1103 | Start Date*: 2011-07-21 |
Sponsor Name:Reckitt Benckiser Healthcare (UK) Ltd | ||
Full Title: A randomised single dose two cohort study comparing the speed of raft formation assessed by gamma scintigraphy in healthy volunteers following administration of a single dose of Gaviscon® Strawberr... | ||
Medical condition: To measure the formation and retention of alginate rafts in healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-002470-42 | Sponsor Protocol Number: 72010 | Start Date*: 2021-11-29 | |||||||||||||||||||||
Sponsor Name:Univeristy Medical Center Utrecht | |||||||||||||||||||||||
Full Title: Sentinel lymph node detection in thyroid carcinoma using [68Ga]Ga-tilmanocept PET/CT: A proof of concept study | |||||||||||||||||||||||
Medical condition: The IMP will be used for the identification of sentinel lymph nodes in patients with thyroid carcinoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003424-12 | Sponsor Protocol Number: CD66-02 | Start Date*: 2007-04-27 | |||||||||||
Sponsor Name:University Hospital Southampton NHS Foundation Trust | |||||||||||||
Full Title: A randomised phase II clinical trial using targeted radiotherapy delivered by an Yttrium-90 radiolabelled Anti-CD66 monoclonal antibody with high dose melphalan compared to melphalan alone, prior t... | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000151-33 | Sponsor Protocol Number: rosu01 | Start Date*: 2007-04-02 | ||||||||||||||||
Sponsor Name:UMCN | ||||||||||||||||||
Full Title: Does caffeine reduce rosuvastatin-induced protection against ischemia-reperfusion injury? | ||||||||||||||||||
Medical condition: Rosuvastatin is a proven cholesterol lowering medicine. Apart from it’s cholesterol lowering action, rosuvastatin may also increase tolerance against ischemia-reperfusion injury. We hypothesize tha... | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
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