- Trials with a EudraCT protocol (48)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
48 result(s) found for: Radius bone.
Displaying page 1 of 3.
EudraCT Number: 2014-005101-21 | Sponsor Protocol Number: GR-OG-279239-01 | Start Date*: 2014-12-22 | |||||||||||
Sponsor Name:Genera Research Ltd | |||||||||||||
Full Title: Safety, tolerability, systemic pharmacokinetics and efficacy of a single dose of Osteogrow (rhBMP6 in autologous Whole Blood Coagulum Derived [WBCD] carrier) delivered locally to the fracture site ... | |||||||||||||
Medical condition: Distal radius fracture. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001041-17 | Sponsor Protocol Number: 20060289 | Start Date*: 2007-09-11 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: An Open Label, Single Arm, Extension Study to Evaluate the Long Term Safety and Sustained Efficacy of Denosumab (AMG162) in the Treatment of Postmenopausal Osteoporosis | |||||||||||||
Medical condition: Treatment of postmenopausal osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) EE (Completed) DE (Completed) LV (Completed) GB (Completed) LT (Completed) HU (Completed) AT (Completed) FI (Completed) BE (Completed) MT (Completed) CZ (Completed) FR (Completed) ES (Completed) GR (Completed) IT (Completed) BG (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005271-15 | Sponsor Protocol Number: 20050179 | Start Date*: 2007-07-18 |
Sponsor Name:Amgen Inc | ||
Full Title: A Multicenter, Randomized Placebo Controlled Pilot MicroCT Study to Estimate the Effect of Treatment with Denosumab (AMG 162) and Alendronate Sodium in Postmenopausal Women with Low Bone Mineral De... | ||
Medical condition: Postmenopausal osteoporosis /osteopenia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-003033-41 | Sponsor Protocol Number: 2005040 | Start Date*: 2006-03-20 | |||||||||||
Sponsor Name:Procter & Gamble Technical Centres Limited | |||||||||||||
Full Title: A Non-invasive Evaluation of Bone Microarchitecture Modification in Osteopenic Postmenopausal Women by 3D Peripheral Quantitative Computed Tomography: A 12 Month, Multicenter, Double-blind, Randomi... | |||||||||||||
Medical condition: Osteoporosis is a systemic skeletal disorder characterized by low bone mass and micro-architectural deterioration of bone tissue leading to enhanced bone fragility and susceptibility to fracture. ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001477-29 | Sponsor Protocol Number: CR9-108914 | Start Date*: 2007-09-10 | |||||||||||
Sponsor Name:GlaxoSmithKline R & D Limited | |||||||||||||
Full Title: A proof-of-concept study of SB-751689 in men and post-menopausal women with a fractured distal radius. | |||||||||||||
Medical condition: Distal radius fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) NL (Prematurely Ended) ES (Completed) CZ (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005598-30 | Sponsor Protocol Number: HMR4003B/3507 | Start Date*: 2006-04-28 | |||||||||||
Sponsor Name:sanofi-aventis Groupe | |||||||||||||
Full Title: A NON-INVASIVE EVALUATION OF BONE MICROARCHITECTURE MODIFICATION IN OSTEOPENIC POSTMENOPAUSAL WOMEN BY 3D-PERIPHERAL QUANTITATIVE COMPUTED TOMOGRAPHY : A 24-MONTH, MONOCENTER, DOUBLE-BLIND, RANDOMI... | |||||||||||||
Medical condition: Osteopenic postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003195-38 | Sponsor Protocol Number: ML 19472 | Start Date*: 2007-09-07 | |||||||||||
Sponsor Name:Center for Muscle and Bone Research of the Charité Universitaetsmedizin Berlin | |||||||||||||
Full Title: Randomized double-blind placebo-controlled and parallel group study to evaluate the impact of one year therapy with monthly oral ibandronate 150 mg on structural properties of bone in postmenopaus... | |||||||||||||
Medical condition: Postmenopausal osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000248-25 | Sponsor Protocol Number: CZOL446O2306 | Start Date*: 2004-08-04 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: A multinational, multicenter, randomized, double-blind, double-dummy, stratified, active controlled parallel group study comparing the efficacy and safety of intravenous zoledronic acid, 5 mg once ... | ||
Medical condition: corticosteroid induced osteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) CZ (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-005096-27 | Sponsor Protocol Number: MBPS205 | Start Date*: 2017-06-23 | |||||||||||
Sponsor Name:Mereo BioPharma 3 Ltd. | |||||||||||||
Full Title: A Phase 2b, Multicentre, Multinational, Double-blind, Dose-finding Study, incorporating an open label substudy, in Adult Patients with Type I, III or IV Osteogenesis Imperfecta Treated with setrusu... | |||||||||||||
Medical condition: Osteogenesis imperfecta | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) GB (GB - no longer in EU/EEA) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006256-22 | Sponsor Protocol Number: 0701104 | Start Date*: 2008-11-21 | |||||||||||
Sponsor Name:CHU Saint-Etienne | |||||||||||||
Full Title: Evaluation by high resolution micro computerized tomography of bone microarchitecture changes in patients with rheumatoid arthritis under anti-TNF therapy. | |||||||||||||
Medical condition: rheumatoid arthritis requiring anti-TNF alpha treatment | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018543-34 | Sponsor Protocol Number: 12153599 | Start Date*: 2010-06-11 | |||||||||||
Sponsor Name:Orthopaedic Syrgery Unit Northern Jytland | |||||||||||||
Full Title: NSAIDs INFLUENCE ON HEAL OF COLLES FRACTURE | |||||||||||||
Medical condition: Ivestigations hypotheses: 1. NSAIDs provide a significant postoperative pain relief that can make mobilization / rehabilitation faster and easier oedema prophylaxis. 2. NSAIDs do not affect bone he... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004220-30 | Sponsor Protocol Number: BA058-05-019 | Start Date*: 2018-07-25 | |||||||||||
Sponsor Name:Radius Health, Inc. | |||||||||||||
Full Title: A Randomized, Double blind, Placebo controlled, Phase 3 Multicenter Study to Evaluate the Safety and Efficacy of Abaloparatide SC for the Treatment of Men with Osteoporosis. | |||||||||||||
Medical condition: Osteoporosis in men | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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: 2019-001650-26 | Sponsor Protocol Number: ZOL6700 | Start Date*: 2019-10-25 |
Sponsor Name:Hospital South West Jutland | ||
Full Title: Zoledronic acid for prevention of bone loss after bariatric surgery | ||
Medical condition: Morbid obese subjects undergoing bariatric surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-010205-37 | Sponsor Protocol Number: 20080098 | Start Date*: 2009-10-28 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo Controlled Study to Compare the Efficacy and Safety of Denosumab versus Placebo in Males with Low Bone Mineral Density | |||||||||||||
Medical condition: Male Osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) FR (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000428-36 | Sponsor Protocol Number: ADJUNCT-1-2021 | Start Date*: 2021-04-21 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Zealand University Hospital, Department of Anaesthesiology | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Oral dexamethasone as an adjunct to a brachial plexus block in patients undergoing orthopaedic surgery of the forearm and hand. A randomised, blinded, placebo-controlled, parallel, triple-arm clini... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Participants undergoing surgery of the bones in the hand or forearm with a lateral infraclavicular brachial plexus block as the means of providing anaesthesia and analgesia will be investigated. We... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-004807-11 | Sponsor Protocol Number: BA058-05-021 | Start Date*: 2020-04-27 | |||||||||||
Sponsor Name:Radius Health Inc. | |||||||||||||
Full Title: A Randomized, Non-Inferiority, Phase 3, Open-Label, Multicenter Study to Evaluate the Efficacy and Safety of Abaloparatide-sMTS for the Treatment of Postmenopausal Women with Osteoporosis | |||||||||||||
Medical condition: Osteoporosis in postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) DK (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000849-19 | Sponsor Protocol Number: 20050234 | Start Date*: 2006-10-27 |
Sponsor Name:Amgen Inc | ||
Full Title: A Randomized Study to Evaluate Safety and Efficacy of Transitioning Therapy From Alendronate to Denosumab (AMG 162) in Postmenopausal Women with Low Bone Mineral Density | ||
Medical condition: Postmenopausal Osteoporosis/osteopenia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: EE (Completed) PT (Prematurely Ended) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-022576-30 | Sponsor Protocol Number: BA058-05-003 | Start Date*: 2011-02-21 | |||||||||||
Sponsor Name:Radius Health, Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Comparative Phase 3 Multicenter Study to Evaluate the Safety and Efficacy of BA058 for Injection for Prevention of Fracture in Ambulatory Postmenopau... | |||||||||||||
Medical condition: Osteoporosis in postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: EE (Completed) LT (Completed) DK (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005991-28 | Sponsor Protocol Number: 20060326 | Start Date*: 2009-06-26 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Randomized, Placebo-controlled, Multi-dose Phase 2 Study to Determine the Efficacy, Safety and Tolerability of AMG 785 in the Treatment of Postmenopausal Women with Low Bone Mineral Density | |||||||||||||
Medical condition: Postmenopausal osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) ES (Completed) DK (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
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