- Trials with a EudraCT protocol (53)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
53 result(s) found for: DEXA scan.
Displaying page 2 of 3.
EudraCT Number: 2008-003748-12 | Sponsor Protocol Number: GESIDA-6008-KRETA | Start Date*: 2008-09-04 |
Sponsor Name:Fundación SEIMC-GESIDA | ||
Full Title: “Estudio Fase IV-III, comparativo, aleatorizado y abierto para evaluar la eficacia para la recuperación de grasa periférica (o de extremidades) de lopinavir/ritonavir en monoterapia versus abacavir... | ||
Medical condition: Infección por el virus de la inmunodeficiencia humana y lipodistrofia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003888-56 | Sponsor Protocol Number: 20192022 | Start Date*: 2021-01-30 | |||||||||||
Sponsor Name:Department of Nephrology, Herlev & Gentofte Hospital, Herlev Hospital | |||||||||||||
Full Title: Treatment of adynamic bone disorder with parathyroid hormone in patients with chronic kidney disease | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002487-41 | Sponsor Protocol Number: GLY-321-2017 | Start Date*: 2018-01-31 | |||||||||||
Sponsor Name:GLyPharma Therapeutic Inc. (a wholly owned subsidiary of VectivBio Holding AG) | |||||||||||||
Full Title: A Phase Ib/IIa open-label, repeated dose, metabolic balance study of FE 203799 in patients with short bowel syndrome | |||||||||||||
Medical condition: Short bowel syndrome (SBS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008208-42 | Sponsor Protocol Number: 08/0168 | Start Date*: 2009-06-26 | |||||||||||
Sponsor Name:UCL - The Joint UCLH/UCL Comprehensive Biomedical Research Unit | |||||||||||||
Full Title: A Randomised, Double-Blind Placebo-Controlled Pilot Study Assessing the Safety and Tolerability of Arimoclomol in Adult with Sporadic Inclusion Body Myositis | |||||||||||||
Medical condition: The research project proposes to investigate Sporadic Inclusion Body Myositis (IBM). IBM is the commonest acquired disease of muscle affecting people aged 50 years and over. It is a progressive and... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023980-17 | Sponsor Protocol Number: Metformin 3.0 | Start Date*: 2011-08-24 |
Sponsor Name:St. Antonius Hospital | ||
Full Title: An efficacy, safety and pharmacokinetic study on the short-term and long-term use of METFORMIN in obese children and adolescents | ||
Medical condition: obese children and adolescents of Caucasian descent with insulin resistance in the age of ≥ 10 and ≤ 16 years at study entry. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012283-14 | Sponsor Protocol Number: SECOND-LINE | Start Date*: 2010-08-16 | |||||||||||
Sponsor Name:National Centre in HIV Epidemiology and Clinical Research | |||||||||||||
Full Title: A randomised open‐label study comparing the safety and efficacy of ritonavir boosted lopinavir and 2‐3N(t)RTI backbone versus ritonavir boosted lopinavir and raltegravir in participants virological... | |||||||||||||
Medical condition: Chronic HIV infection | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) FR (Ongoing) GB (Completed) DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003932-35 | Sponsor Protocol Number: BIO101-CL03 | Start Date*: 2018-02-20 | |||||||||||
Sponsor Name:Biophytis S.A. | |||||||||||||
Full Title: Safety and Efficacy of BIO-101 175 mg b.i.d. and 350 mg b.i.d. 26-week oral administration to patients suffering from age-related SARcopenia, including sarcopenic obesity, Aged ≥65 years and at ris... | |||||||||||||
Medical condition: Sarcopenia including sarcopenic obesity | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000550-12 | Sponsor Protocol Number: 2014-PT026 | Start Date*: 2014-07-23 | |||||||||||
Sponsor Name:XBiotech Germany GmbH | |||||||||||||
Full Title: A Double Blind, Placebo Controlled, Pivotal Phase III Study Evaluating Xilonix™ in Symptomatic Colorectal Cancer Patients Refractory To Standard Therapy | |||||||||||||
Medical condition: Symptomatic Colorectal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) PL (Completed) DE (Prematurely Ended) CZ (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001266-17 | Sponsor Protocol Number: DMD114349 | Start Date*: 2011-08-08 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development LTD | |||||||||||||
Full Title: An open-label extension study of the long-term safety, tolerability and efficacy of GSK2402968 in subjects with Duchenne Muscular Dystrophy | |||||||||||||
Medical condition: Duchenne Muscular Dystrophy | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: BE (Prematurely Ended) FR (Ongoing) DE (Completed) GB (Prematurely Ended) NL (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) Outside EU/EEA BG (Prematurely Ended) HU (Prematurely Ended) DK (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005390-21 | Sponsor Protocol Number: IBDCL-GELTAMO-2015 | Start Date*: 2016-02-19 | |||||||||||
Sponsor Name:GELTAMO | |||||||||||||
Full Title: Multicentric phase II trial to evaluate the efficacy and safety of Ibrutinib in combination with rituximab, gemcitabine, oxaliplatin and dexamethasone followed by Ibrutinib maitenance in patients w... | |||||||||||||
Medical condition: diffuse large B-cell lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000299-13 | Sponsor Protocol Number: NVD003-CLN01 | Start Date*: 2018-05-17 |
Sponsor Name:Novadip Biosciences | ||
Full Title: A prospective multicentre single-arm study in adults to evaluate the safety and preliminary efficacy of the autologous 3D osteogenic implant NVD-003 for bone reconstruction for the treatment of rec... | ||
Medical condition: Patients with documented recalcitrant lower limb nonunion, meaning a single, meta- and/or diaphyseal nonunion defect of femur or tibia after at least one failed reconstructive surgical attempt. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) LU (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004766-34 | Sponsor Protocol Number: CLCI699C2301 | Start Date*: 2014-08-01 |
Sponsor Name:NOVARTIS FARMA S.p.A. | ||
Full Title: A Phase III, multi-center, double-blind, randomized withdrawal study of LCI699 following a 24 week, single-arm, open-label dose titration and treatment period to evaluate the safety and efficacy of... | ||
Medical condition: Cushing's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) GB (Completed) DE (Completed) AT (Completed) ES (Completed) NL (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003417-32 | Sponsor Protocol Number: NN2211-1572 | Start Date*: 2006-05-08 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Liraglutide Effect and Action in Diabetes (LEAD-2): Effect on glycaemic control after once daily administration of liraglutide in combination with metformin versus metformin monotherapy versus metf... | |||||||||||||
Medical condition: Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) HU (Completed) SE (Completed) DK (Completed) GB (Completed) SK (Completed) BE (Completed) ES (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003708-11 | Sponsor Protocol Number: GS-US-236-0128 | Start Date*: 2012-11-05 | |||||||||||
Sponsor Name:Gilead Sciences Incorporated | |||||||||||||
Full Title: A Randomized, Double-blind Phase 3B Study to Evaluate the Safety and Efficacy of Elvitegravir/Cobicistat/Emtricitabine/Tenofovir Disoproxil Fumarate Versus Ritonavir-Boosted Atazanavir Plus Emtrici... | |||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV-1) Infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) PT (Completed) IT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017169-53 | Sponsor Protocol Number: BAY86-5258/13788 | Start Date*: 2011-01-17 | |||||||||||
Sponsor Name:Bayer HelathCare AG | |||||||||||||
Full Title: Estudio multicéntrico, abierto, de un brazo de tratamiento para evaluar la seguridad y la eficacia de la administración oral diaria de 2 mg de Dienogest en el tratamiento de la endometriosis en ado... | |||||||||||||
Medical condition: Sospecha clínica o confirmada de endometriosis en mujeres adolescentes post-menarquia de 12 a menos de 18 años de edad (Clinically suspected or confirmed endometriosis in post menarche female adole... | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) FI (Completed) DE (Completed) AT (Completed) FR (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001641-33 | Sponsor Protocol Number: PETAL-Studie | Start Date*: 2007-07-25 |
Sponsor Name:Universitätsklinikum Essen | ||
Full Title: Positronen-Emissionstomographie-gesteuerte Therapie aggressiver Non-Hodgkin-Lymphome (Positron emission tomography guided therapy of aggressive non-Hodgkin's lymphomas) | ||
Medical condition: Aggressive non-Hodgkin's lymphomas (first line therapy) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004934-40 | Sponsor Protocol Number: 20072651 | Start Date*: 2021-03-19 | |||||||||||
Sponsor Name:Department of Endocrinology and Internal Medicine, Aarhus University Hospital | |||||||||||||
Full Title: Endocrine, cardiovascular, pharmacologic and physiologic aspects of sex hormone treatment in Turner syndrome - project part B | |||||||||||||
Medical condition: Ovarian dysgenesis and related hypogonadism causes by Turner syndrome | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004497-15 | Sponsor Protocol Number: ERGO | Start Date*: 2016-12-12 | |||||||||||
Sponsor Name:UMBERTO I - POLICLINICO DI ROMA | |||||||||||||
Full Title: Study on New Insights in Remodeling of Endocrine Cardiomyopathies: Intramyocardial, Molecular and Neuroendocrine Assessment in Response to Chronic Inhibition of Cyclic GMP Phosphodiesterase 5A in C... | |||||||||||||
Medical condition: Cushing’s Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002486-21 | Sponsor Protocol Number: GLY-311-2017 | Start Date*: 2018-01-18 | |||||||||||
Sponsor Name:GLyPharma Therapeutic, Inc. (a wholly owned subsidiary of VectivBio Holding AG) | |||||||||||||
Full Title: A once weekly, repeated dose, placebo controlled, double blind, randomised cross-over trial investigating safety, efficacy and pharmacodynamics of FE 203799 in patients with short bowel syndrome wi... | |||||||||||||
Medical condition: Short Bowel Syndrome (SBS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004498-34 | Sponsor Protocol Number: SUM | Start Date*: 2016-12-12 | |||||||||||
Sponsor Name:UMBERTO I - POLICLINICO DI ROMA | |||||||||||||
Full Title: Study on New Insights in Remodeling of Endocrine Cardiomyopathies: ASsessmentt of Intramyocardial, Molecular and NeUroendocrine Parameters in Response to Chronic Inhibition of Cyclic GMP Phosphodie... | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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