- Trials with a EudraCT protocol (30)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
30 result(s) found for: Humerus.
Displaying page 1 of 2.
EudraCT Number: 2011-005801-54 | Sponsor Protocol Number: 1 | Start Date*: 2012-02-22 | |||||||||||
Sponsor Name:Hvidovre Hospital | |||||||||||||
Full Title: The effect of 1-84 parathyroidhormone in the treatment of proximal fracture of the humerus. | |||||||||||||
Medical condition: Fracture of proximal humerus | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001916-54 | Sponsor Protocol Number: 3100N7-212-WW | Start Date*: 2007-01-16 | |||||||||||
Sponsor Name:Wyeth Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Double-Blind, Randomized, Stratified, Controlled, Efficacy, Safety and Feasibility Study of rhBMP-2/CPM as an Adjuvant Therapy in Closed Fractures of the Humerus | |||||||||||||
Medical condition: Closed Fractures of the Humerus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) FR (Completed) SE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004047-23 | Sponsor Protocol Number: 273551-2 | Start Date*: 2019-12-05 |
Sponsor Name:University of Bergen | ||
Full Title: Evaluation of safety and feasibility of autologous MSCs combined to biomaterial to enhance bone healing in patients with delayed consolidation after long bone defects requiring graft apposition or ... | ||
Medical condition: Diaphyseal and/or metaphysodiaphyseal fractures (femur, tibia, humerus) status delayed union (after 3 months) treated by standard care procedures | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005441-13 | Sponsor Protocol Number: C11-12 | Start Date*: 2013-01-03 | |||||||||||
Sponsor Name:INSERM | |||||||||||||
Full Title: Evaluation of efficacy and safety of autologous MSCs combined to biomaterials to enhance bone healing in patients with delayed consolidation after long bone fracture requiring graft apposition or ... | |||||||||||||
Medical condition: Closed or open Gustilo I ans II humerus, tibial or femur diaphyseal or metaphysodiaphyseal fracture. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002154-39 | Sponsor Protocol Number: VINFORCE007 | Start Date*: 2014-10-23 | |||||||||||
Sponsor Name:Vinforce - Institut für Osteoporoseforschung [...] | |||||||||||||
Full Title: Teriparatide for fracture repair in humans: A prospective, randomized, double-blind placebo-controlled pilot study in female and male patients with proximal humerus fracture The TERAFRAP Study | |||||||||||||
Medical condition: Osteoporotic humerus fracture - accelerated fracture repair | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002961-21 | Sponsor Protocol Number: NS918 | Start Date*: 2018-11-09 |
Sponsor Name:UZ Leuven | ||
Full Title: The effect of deep neuromuscular block and reversal with sugammadex on surgical conditions and perioperative morbidity in shoulder surgery using a deltopectoral approach | ||
Medical condition: Subject undergoing elective or semi-elective surgery to the gleno-humeral joint or the proximal humerus using a deltoideo-pectoral approach. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001456-11 | Sponsor Protocol Number: 20070337 | Start Date*: 2012-04-17 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Multicenter, International, Randomized, Double-blind, Placebo controlled, Parallel-group Study to Assess the Efficacy and Safety of Romosozumab Treatment in Postmenopausal Women With Osteoporosis | |||||||||||||
Medical condition: Postmenopausal Osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) DK (Completed) PL (Completed) DE (Completed) GB (Completed) EE (Completed) CZ (Completed) ES (Completed) LV (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003142-41 | Sponsor Protocol Number: 20110142 | Start Date*: 2012-03-28 | |||||||||||
Sponsor Name:AMGEN INC. | |||||||||||||
Full Title: A Multicenter, International, Randomized, Double-blind, Alendronate-controlled Study to Determine the Efficacy and Safety of AMG 785 in the Treatment of Postmenopausal Women With Osteoporosis | |||||||||||||
Medical condition: Postmenopausal osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) LT (Completed) FI (Completed) PL (Completed) BE (Completed) CZ (Completed) ES (Completed) EE (Completed) GR (Completed) DE (Completed) GB (Completed) SE (Completed) AT (Completed) DK (Completed) LV (Completed) NO (Completed) NL (Completed) HU (Completed) IE (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000431-32 | Sponsor Protocol Number: ORTHOUNION | Start Date*: 2017-05-25 | ||||||||||||||||
Sponsor Name:Universidad Autónoma de Madrid (U.A.M.) | ||||||||||||||||||
Full Title: A MULTI-CENTRE, OPEN-LABEL, RANDOMIZED, COMPARATIVE CLINICAL TRIAL OF TWO DIFFERENT DOSES OF BONE MARROW AUTOLOGOUS HUMAN MESENCHYMAL STEM CELLS PLUS BIOMATERIAL VERSUS ILIAC CREST AUTOLOGOUS GRAFT... | ||||||||||||||||||
Medical condition: Diaphyseal and/or metaphysodiaphyseal fractures (femur, tibia, humerus) with status of non-union | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) DE (Completed) FR (Ongoing) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000123-41 | Sponsor Protocol Number: B3D-EW-GHDW | Start Date*: 2012-09-20 | |||||||||||
Sponsor Name:Eli Lilly and Company Limited | |||||||||||||
Full Title: Teriparatide and Risedronate in the Treatment of Patients with Severe Postmenopausal Osteoporosis: Comparative Effects on Vertebral Fractures | |||||||||||||
Medical condition: Postmenopausal women with established osteoporosis and at least two moderate or one severe prevalent fragility fracture. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) BE (Completed) ES (Completed) DE (Completed) AT (Completed) IT (Completed) HU (Completed) GR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004219-36 | Sponsor Protocol Number: MR-ISB-1 | Start Date*: 2013-12-02 |
Sponsor Name:Paracelsus Mediznische Privatuniversität, Universitätsklinik für Anästhesiologie, perioperative Medizin und Intensiv | ||
Full Title: Magnetic Resonance Imaging of Local Anesthetic Distribution: A Comparison of 5 and 15 milliliters of ropivacaine 0.75% for ultrasound guided interscalene plexus blockade | ||
Medical condition: Surgery of the shoulder and/or upper extremity using interscalene brachial plexus block | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003813-24 | Sponsor Protocol Number: SIFU17 | Start Date*: 2019-11-28 |
Sponsor Name:Charité-Universitätsmedizin Berlin | ||
Full Title: A phase I/IIa, prospective, mono-center, randomized, open labeled, controlled study to assess the safety and efficacy of applying Iloprost locally in the fracture site to promote bone healing in pa... | ||
Medical condition: Proximal humeral fracture | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003479-20 | Sponsor Protocol Number: 2011/433 | Start Date*: 2013-04-15 | |||||||||||
Sponsor Name:Handkirurgiska kliniken, Universitetssjukhuset Örebro | |||||||||||||
Full Title: Lateral humerus epicondylitis- a clinical, muscle morpological, muscle metabolical and functional evaluation of a new model for treatment. | |||||||||||||
Medical condition: Chronic lateral humerus epiconcylitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000094-37 | Sponsor Protocol Number: FAO_06_011 | Start Date*: 2008-05-06 | |||||||||||
Sponsor Name:Glostrup University Hospital | |||||||||||||
Full Title: Effect of PTH(1-34)-treatment on fracture healing in vivo | |||||||||||||
Medical condition: pertrocanteric femur fractures or collum humerus fractures in osteoporotic postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001820-51 | Sponsor Protocol Number: BMC2012-PhaseII | Start Date*: 2016-06-27 |
Sponsor Name:Dekan der medizinischen Fakultät, Universitätsklinikum Frankfurt, Goethe-Universität | ||
Full Title: BMC2012, Cell based therapy by implanted bone marrow-derived mononuclear cells (BMC) for bone augmentation of plate-stabilized proximal humeral fractures - a randomized, open, multicentric study - ... | ||
Medical condition: Investigation of cell based therapy by implanted bone marrow-derived mononuclear cells for bone augmentation on osteosynthesis of proximal humeral fractures | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000930-37 | Sponsor Protocol Number: STEMQUIRI/12ES01 | Start Date*: 2014-04-29 | |||||||||||
Sponsor Name:Laboratorios Salvat, S.A. | |||||||||||||
Full Title: A phase II clinical trial to assess the effect of HC-SVT-1001 (autologous fat stem adult mesenchymal cells expanded and combined with a tricalcium phosphate biomaterial) and HC-SVT-1002 (allogeneic... | |||||||||||||
Medical condition: Atrophic pseudarthrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001249-41 | Sponsor Protocol Number: KEK-ZH-2012-0249 | Start Date*: 2013-04-12 |
Sponsor Name:University Hospital of Zurich and City Hospital Waid | ||
Full Title: Vitamin D3 – Omega3 – Home Exercise – HeALTHy Ageing and Longevity Trial Randomized, double-blind, placebo-controlled, multi-centre clinical trial | ||
Medical condition: healthy ageing, functional decline | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) PT (Completed) FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001921-29 | Sponsor Protocol Number: BA058-05-007 | Start Date*: 2012-08-13 | |||||||||||
Sponsor Name:Radius Health Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study of BA058 Administered via a Coated Transdermal Microarray Delivery System (BA058 Transdermal) in Healthy Postmenopausal Women with Oste... | |||||||||||||
Medical condition: Osteoporosis in postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: PL (Completed) EE (Completed) DK (Completed) LT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004875-12 | Sponsor Protocol Number: PRPEPI2013 | Start Date*: 2014-09-24 | |||||||||||
Sponsor Name:Fakultní nemocnice Ostrava | |||||||||||||
Full Title: Application of PRP (plattelet rich plasma) to the lateral epicondyle of the humerus | |||||||||||||
Medical condition: Lateral epicondylitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005712-22 | Sponsor Protocol Number: 01-2020 | Start Date*: 2021-07-08 | |||||||||||
Sponsor Name:Gedeon Richter Ibérica | |||||||||||||
Full Title: Prospective, randomized, multicenter study to compare the efficacy at 52 weeks (1 year) of biosimilar teriparatide and alendronate in the prevention of new morphometric vertebral fractures and / or... | |||||||||||||
Medical condition: Osteoporosis in postmenopausal women at increased risk of fracture. | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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