- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Mathematical model.
Displaying page 1 of 1.
| EudraCT Number: 2014-005473-36 | Sponsor Protocol Number: Dezember2014Version2 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Universitätsklinikum Freiburg | ||
| Full Title: Modeling of lipoprotein in patients with familial hypercholesterolemia compared to healthy subjects | ||
| Medical condition: familial hypercholesterolemia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-005135-24 | Sponsor Protocol Number: ECDOPDEP2013 | Start Date*: 2014-03-21 | |||||||||||
| Sponsor Name:Cristina Fernandez Pérez | |||||||||||||
| Full Title: Clinical Trial crossed athletic population according UGT2B17 polymorphism. Impact on the steroid profile | |||||||||||||
| Medical condition: Sports doping | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003551-30 | Sponsor Protocol Number: August2016 | Start Date*: 2017-03-02 | |||||||||||
| Sponsor Name:Universitätsklinikum Freiburg | |||||||||||||
| Full Title: Modeling of the impact of a PCSK9 inhibition on lipoproteins in patients with dyslipidemia | |||||||||||||
| Medical condition: dyslipidemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000077-68 | Sponsor Protocol Number: CAMN107ADE18T | Start Date*: 2013-12-10 | ||||||||||||||||
| Sponsor Name:Medical Center - University of Freiburg | ||||||||||||||||||
| Full Title: Imatinib continuation versus Nilotinib 300 mg twice daily in patients with chronic myeloid leukemia (CML) in chronic phase and major molecular response (MMR) without molecular response ≥ 4.5 log (M... | ||||||||||||||||||
| Medical condition: chronic myeloid leukemia (CML) in 1st chronic phase and confirmed major molecular response (MMR) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-002483-26 | Sponsor Protocol Number: 1998/2005 | Start Date*: 2005-12-01 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
| Full Title: Tailoring antiviral therapy of chronic hepatitis C to the single patient standard therapy versus treatment guided by a physic-mathematical model of the dynamics of Hepatitis C Virus infection. | |||||||||||||
| Medical condition: Chronic Hepatitis C with or without cirrhosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004833-25 | Sponsor Protocol Number: UNLOCK | Start Date*: 2017-03-29 |
| Sponsor Name:Consorci Mar Parc de Salut de Barcelona (Parc de Salut Mar) | ||
| Full Title: Synchronous effect of anesthetics on fMRI, EEG and clinical responses. Development of a more precise system for monitoring anesthetic effect. | ||
| Medical condition: General anaesthesia in healthy subjects | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-002318-15 | Sponsor Protocol Number: 010921 | Start Date*: 2021-09-15 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Copenhagen University Hospital, Amager and Hvidovre, Department of Clinical Research | ||||||||||||||||||||||||||||||||||||||
| Full Title: A pharmacological trial with Sativex® and gentamicin for optimized pharmacological treatment of older patients with a focus on appetite stimulation and renal risk drugs | ||||||||||||||||||||||||||||||||||||||
| Medical condition: | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2019-003087-43 | Sponsor Protocol Number: SAFER | Start Date*: 2021-01-12 | |||||||||||
| Sponsor Name:Synektik Spółka Akcyjna | |||||||||||||
| Full Title: A Phase I/II Seamless Adaptive, Open label study to assess Safety, Tolerability, Radiation Dosimetry, Biodistribution, and diagnostic ability of a Novel 18F-labelled Tracer, SYN2, for Positron Emis... | |||||||||||||
| Medical condition: phase II: suspected coronary artery disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-014406-34 | Sponsor Protocol Number: ORVACS-010 | Start Date*: 2010-05-28 | |||||||||||
| Sponsor Name:ORVACS | |||||||||||||
| Full Title: International, multicenter, randomized, non-comparative controlled study of therapeutic intensification plus immunomodulation in HIV patients with long-term viral suppression | |||||||||||||
| Medical condition: HIV-1 Infection | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) GB (Completed) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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