- Trials with a EudraCT protocol (78)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (67)
78 result(s) found for: Choline.
Displaying page 1 of 4.
EudraCT Number: 2013-003058-25 | Sponsor Protocol Number: 1320 | Start Date*: 2013-11-05 |
Sponsor Name:University Hospital Grenoble | ||
Full Title: PREMATURE EVALUATION OF THE ANSWER BY TEP HAS THE CHOLINE IN THE METASTATIC PROSTATE CANCER | ||
Medical condition: METASTATIC PROSTATE CANCER | ||
Disease: | ||
Population Age: | Gender: Male | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004828-23 | Sponsor Protocol Number: CR0701-21 | Start Date*: 2010-04-01 | |||||||||||
Sponsor Name:Cancer Research UK | |||||||||||||
Full Title: A Cancer Research UK Phase II Trial to compare [11C]choline and [18F]choline each given as a single administration via intravenous injection for imaging patients with metastatic prostate cancer | |||||||||||||
Medical condition: metastatic prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003933-33 | Sponsor Protocol Number: 12K3-S-140708 | Start Date*: 2006-12-20 |
Sponsor Name:Bundeswehr | ||
Full Title: Clinical value of Choline-Positron-Emission-Tomography combined with Magnetic Resonance Imaging by software fusion for pre-therapeutic staging of prostate cancer | ||
Medical condition: Clinical value of Choline-Positron-Emission-Tomography combined with Magnetic Resonance Imaging by software fusion for pre-therapeutic staging of prostate cancer referring to histopathological, pos... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001961-34 | Sponsor Protocol Number: RDG-1/PBC | Start Date*: 2021-02-02 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomised, placebo-controlled, phase II dose-finding study comparing different doses of RhuDex granules with placebo in the treatment of primary biliary cholangitis | |||||||||||||
Medical condition: Primary biliary cholangitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) HU (Prematurely Ended) SK (Prematurely Ended) NL (Prematurely Ended) BE (Completed) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001330-17 | Sponsor Protocol Number: PET-COLINA_2013 | Start Date*: 2013-06-23 | |||||||||||
Sponsor Name:IRCCS Azienda Ospedaliera Universitaria San Martino – IST Istituto Nazionale per la Ricerca sul Cancro | |||||||||||||
Full Title: Comparison between diagnostic accuracy of [11C]-choline PET/CT and conventional imaging in prostate cancer patients | |||||||||||||
Medical condition: Prostate adenocarcinoma accounts for 11% of all malignancies, with a total 2.6 million new cases / year estimated in Europe. Mortality rate is 30.6 / 100,000 persons/year. Prostate cancer general... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000411-40 | Sponsor Protocol Number: Version1.0 | Start Date*: 2015-10-23 |
Sponsor Name:Department of Nuclear Medicine and Endocrinology, Paracelsus Medical University Salzburg | ||
Full Title: Comparison of the detection of parathyroid adenoms using Tc-99m MIBI scintigraphy and F-18 Choline PET/CT in patients with primary hyperparathyroidism | ||
Medical condition: Primary hyperparathyroidism due to parathyroid adenoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004215-50 | Sponsor Protocol Number: C601 | Start Date*: 2019-04-23 | |||||||||||
Sponsor Name:Soleno Therapeutics UK Ltd. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study of Diazoxide Choline Controlled-Release Tablet (DCCR) in Patients with Prader-Willi Syndrome | |||||||||||||
Medical condition: Hyperphagia associated with Prader-Willi Syndrome. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001064-37 | Sponsor Protocol Number: S348.2.001 | Start Date*: 2008-07-31 | |||||||||||
Sponsor Name:Fournier Laboratories Ireland | |||||||||||||
Full Title: Effect of Choline Fenofibrate (ABT-335 /SLV348) on Macular Edema Measured by Optical Coherence Tomography in Subjects with Diabetic Macular Edema - a one-year, Placebo-Controlled, Randomized Study | |||||||||||||
Medical condition: Diabetic macular edema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Completed) NL (Completed) GB (Completed) ES (Completed) HU (Completed) AT (Prematurely Ended) DK (Completed) IT (Completed) BG (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003027-21 | Sponsor Protocol Number: RM2-01-01-14 | Start Date*: 2015-03-30 | |||||||||||
Sponsor Name:Piramal Imaging SA | |||||||||||||
Full Title: Open-label, multi center PET/CT (positron emission tomography/computed tomography) study for investigation of safety and diagnostic performance of the 68Ga labeled PET tracer [68Ga]RM2 following a ... | |||||||||||||
Medical condition: Patients with primary prostate cancer in which prostate cancer is histologically confirmed and a prostatectomy is planned. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: AT (Prematurely Ended) FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003188-13 | Sponsor Protocol Number: CONIVAD | Start Date*: 2016-09-23 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA CAREGGI | |||||||||||||
Full Title: Pilot study on the association choline alphoscerate-nimodipine in patients with subcortical vascular cognitive impairment | |||||||||||||
Medical condition: Subcortical vascular cognitive impairment | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011556-22 | Sponsor Protocol Number: AU 03/2009 | Start Date*: 2009-05-07 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS OSPEDALE MAGGIORE POLICLINICO MANGIAGALLI E REGINA ELENA | |||||||||||||
Full Title: Treatment of sudden idiopathic deafness with hyperbaric oxygen-therapy and intramuscular injection of CDP-choline. | |||||||||||||
Medical condition: NONE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004216-22 | Sponsor Protocol Number: C602 | Start Date*: 2019-09-25 | |||||||||||
Sponsor Name:Soleno Therapeutics UK Ltd. | |||||||||||||
Full Title: An Open-Label, Long-Term Safety and Efficacy Evaluation of Diazoxide Choline Controlled-Release Tablet in Patients with Prader-Willi Syndrome | |||||||||||||
Medical condition: Hyperphagia associated with Prader-Willi Syndrome (PWS) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004907-39 | Sponsor Protocol Number: D0170C00009 | Start Date*: 2005-03-04 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Phase II, double-blind, randomized, cross-over, international, multicentre study to evaluate the analgesic efficacy of 3 weeks oral administration of AZD4282 300 mg b.i.d. compared with placebo i... | ||
Medical condition: Diagnostic of Post Traumatic Neuralgia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004951-38 | Sponsor Protocol Number: Pet-Col | Start Date*: 2011-10-10 | |||||||||||
Sponsor Name:AZIENDA USL DI FORLI' | |||||||||||||
Full Title: Role of PET/CT with 18F-choline in biochemical relapse in prostate cancer patients treated with radical intent. Pet Col study. | |||||||||||||
Medical condition: prostate cancer patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005262-39 | Sponsor Protocol Number: 2006-2209 | Start Date*: 2007-05-30 |
Sponsor Name:Charité-Universitätsmedizin Berlin | ||
Full Title: Flupirtin as Oral Treatment in MS | ||
Medical condition: Relapsing-remitting multiple sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-004908-21 | Sponsor Protocol Number: D0170C00006 | Start Date*: 2005-02-28 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Phase II, double-blind, randomized, cross-over, international, multicentre study to evaluate the analgesic efficacy of 3 weeks oral administration of AZD4282 300 mg b.i.d. compared with placebo i... | ||
Medical condition: Diagnosis of postherpetic neuralgia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-002578-36 | Sponsor Protocol Number: 2008/0817 | Start Date*: 2008-09-10 |
Sponsor Name:CHRU de LILLE | ||
Full Title: Etude d’efficacité et d’acceptabilité d’un traitement cholinergique dans l’apathie parkinsonienne “Cholinergic treatment in Parkinsonian Apathy: ChoPA - I” | ||
Medical condition: Parkinsonian Apathy without dementia and depression in spite of dopaminergic treatment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003165-15 | Sponsor Protocol Number: FACBC-STAGING-2014 | Start Date*: 2014-12-02 | |||||||||||
Sponsor Name:AOU di Bologna Policlinico S.Orsola-Malpighi | |||||||||||||
Full Title: 18F-FACBC PET/CT FOR STAGING HIGH RISK PROSTATE CANCER | |||||||||||||
Medical condition: Patients affected by moderate to high risk primary prostate cancer who are scheduled for surgery with a planned, elective lymph node dissection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000576-38 | Sponsor Protocol Number: CARL | Start Date*: 2022-06-08 | |||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI CAMERINO | |||||||||||||
Full Title: Effect of treatment of the cholinergic precursor Choline Alfoscerate in mild cognitive dysfunction | |||||||||||||
Medical condition: Mild cognitive dysfunction | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003437-10 | Sponsor Protocol Number: CARTESIO | Start Date*: 2023-04-05 | |||||||||||
Sponsor Name:Azienda Socio Sanitaria Territoriale di Lodi | |||||||||||||
Full Title: PILOT STUDY ON THE EFFECTIVENESS OF CHOLINE ALFOSCERATE IN THE UNDER THRESHOLD DEPRESSION OF THE ELDERLY | |||||||||||||
Medical condition: Under threshold depression of the elderly. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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