- Trials with a EudraCT protocol (235)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
235 result(s) found for: Bone Fracture.
Displaying page 1 of 12.
| EudraCT Number: 2015-001458-14 | Sponsor Protocol Number: P130921 | Start Date*: 2015-10-01 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002143-27 | Sponsor Protocol Number: 73950 | Start Date*: 2021-02-09 | |||||||||||
| Sponsor Name:Maasstad Ziekenhuis | |||||||||||||
| Full Title: Spinal morphine in patients with hip fractures to reduce delirium | |||||||||||||
| Medical condition: Proximal femur fracture | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2008-002098-11 | Sponsor Protocol Number: RC 30\07 | Start Date*: 2009-06-25 | |||||||||||
| Sponsor Name:ISTITUTO PER L'INFANZIA BURLO GAROFOLO | |||||||||||||
| Full Title: Randomized Controlled Trial on the effectiveness of ketorolac and tramadole in not compound fractures of child. | |||||||||||||
| Medical condition: Not compound fractures in childhood. | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2008-004964-38 | Sponsor Protocol Number: Trauma-fenta version 1 | Start Date*: 2008-12-29 | |||||||||||
| Sponsor Name:Kari Leino | |||||||||||||
| Full Title: Perioperative pain treatment with fentanyl patch in trauma patients having an ankle or crural fracture/ Nilkka- ja säärimurtumapotilaiden perioperatiivinen kivunhoito fentanyylilaastarilla | |||||||||||||
| Medical condition: Patients having an ankle or crural fracture will be included. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 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: 2011-000988-28 | Sponsor Protocol Number: 19403 | Start Date*: 2011-08-16 | |||||||||||
| Sponsor Name:University of Edinburgh [...] | |||||||||||||
| Full Title: Fractures and Bisphosphonates: A double-blind, randomised controlled trial on the effect of alendronic acid on healing and clinical outcomes of wrist fractures | |||||||||||||
| Medical condition: Fracture healing | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-015939-33 | Sponsor Protocol Number: 20080394 | Start Date*: 2010-03-23 |
| Sponsor Name:Amgen Inc | ||
| Full Title: A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults with Fresh Unilateral Intertrochanteric Fracture of the P... | ||
| Medical condition: Acceleration of fracture healing | ||
| Disease: | ||
| Population Age: | Gender: Male, Female | |
| Trial protocol: FR (Completed) GB (Completed) DE (Completed) SE (Completed) PL (Completed) DK (Completed) NL (Completed) LV (Completed) GR (Completed) IT (Completed) HU (Completed) BE (Completed) FI (Completed) LT (Completed) EE (Completed) BG (Completed) SI (Completed) | ||
| Trial results: View results | ||
| 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: 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: 2011-005801-54 | 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: 2015-000654-38 | Sponsor Protocol Number: AHUS2015-000654-38 | Start Date*: 2015-10-19 | |||||||||||
| Sponsor Name:Akershus University Hospital, Norway | |||||||||||||
| Full Title: Secondary prophylaxis after hip fracture. An evaluation og two organisational models based on choise of treatment: a comparison of efficacy and applicability of hospital based treatment with zoled... | |||||||||||||
| Medical condition: Hip fracture | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-017039-16 | Sponsor Protocol Number: CL3-12911-036 | Start Date*: 2010-05-05 | ||||||||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier | ||||||||||||||||||
| Full Title: Effect of strontium ranelate (2g per day) in the management of long bone fractures with delayed-union or non union: an international open label study | ||||||||||||||||||
| Medical condition: Delayed and non-united fractures | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: CZ (Completed) HU (Completed) FR (Completed) IT (Completed) DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-001543-13 | Sponsor Protocol Number: HIP-SAP | Start Date*: 2018-03-28 | ||||||||||||||||||||||||||
| Sponsor Name:Morten Tange Kristensen/Hvidovre Hospital | ||||||||||||||||||||||||||||
| Full Title: Preliminary effect and safety of physiotherapy with strength training and protein-dense nutritional supplement in combination with anabolic steroids in cross-continuum rehabilitation of patients wi... | ||||||||||||||||||||||||||||
| Medical condition: Area of investigation is recovery of muscle strength and function following hip fracture surgery. | ||||||||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2018-001054-96 | Sponsor Protocol Number: 000013/BT | Start Date*: 2020-03-19 | |||||||||||
| Sponsor Name:Bone Therapeutics S.A. | |||||||||||||
| Full Title: Phase IIb, Placebo-Controlled, Randomized, Double-blind, Multicenter Study to Assess the Efficacy and Safety of Allogeneic Osteoblastic Cells (ALLOB) Single Implantation in Tibial Fracture | |||||||||||||
| Medical condition: Tibial fracture considered at risk of DU/NU (based on the combination of risk factors documented to be associated with increased proportion of DU/NU). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) FR (Completed) DE (Prematurely Ended) HU (Prematurely Ended) PL (Prematurely Ended) ES (Ongoing) CZ (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001831-23 | Sponsor Protocol Number: 3100N7-210 WW | Start Date*: 2007-01-23 | |||||||||||
| Sponsor Name:Wyeth Pharmaceuticals Inc. | |||||||||||||
| Full Title: A Phase 2/3, Multicenter, Double-Blind, Randomized, Controlled Study of Recombinant Human Bone Morphogenetic Protein-2 (rhBMP 2)/Calcium Phosphate Matrix (CPM) in Closed Diaphyseal Tibial Fractures | |||||||||||||
| Medical condition: Closed diaphyseal tibial fracture | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) SE (Completed) DE (Prematurely Ended) FI (Completed) GB (Completed) LV (Completed) SI (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001455-35 | Sponsor Protocol Number: P051033 | Start Date*: 2006-11-09 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Intérêt de l'association du midazolam par voie sublinguale à la morphine par voie orale dans l'analgésie des fractures déplacées de l'enfant aux urgences | |||||||||||||
| Medical condition: Facture déplacée chez l'enfant | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003688-30 | Sponsor Protocol Number: CS I-040101/02 | Start Date*: 2007-02-27 | |||||||||||
| Sponsor Name:Kuros Biosurgery AG | |||||||||||||
| Full Title: A phase 2 randomized, controlled, open-label (dose-blinded), multi-center, dose-finding study of the safety and efficacy of I-0401 in the treatment of patients with fractures of the tibial plateau ... | |||||||||||||
| Medical condition: Fractures of the tibial plateau requiring grafting | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) ES (Completed) IT (Completed) FR (Completed) HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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