- Trials with a EudraCT protocol (50)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
50 result(s) found for: Fracture healing.
Displaying page 1 of 3.
EudraCT Number: 2009-014271-41 | Sponsor Protocol Number: CL3-12911-035 | Start Date*: 2010-03-16 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: A multicenter, prospective, randomized, double-blind, placebo-controlled, international study to assess the effects of 2g per day of strontium ranelate versus placebo on the time to fracture healin... | |||||||||||||
Medical condition: Osteoporotic men and post menopausal osteoporotic women with a fracture of the distal radius | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) IT (Completed) HU (Completed) GB (Completed) BE (Completed) | |||||||||||||
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 (Ongoing) DE (Prematurely Ended) HU (Prematurely Ended) PL (Prematurely Ended) ES (Ongoing) CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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: 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: 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) |
EudraCT Number: 2008-008392-34 | Sponsor Protocol Number: 20062017 | Start Date*: 2009-08-27 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Multi-center, Randomized, Double-blind, Placebo-controlled Study of AMG 785 in Skeletally Mature Adults with a Fresh Unilateral Tibial Diaphyseal Fracture Status Post Definitive Fracture Fixation... | |||||||||||||
Medical condition: Acceleration of fracture healing | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) DK (Completed) GB (Completed) DE (Completed) FR (Completed) GR (Completed) IT (Completed) BG (Completed) HU (Completed) LT (Completed) EE (Completed) NO (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: 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: 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: 2011-001116-65 | Sponsor Protocol Number: B3D-MC-GHDQ | Start Date*: 2012-02-10 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Second study on the Effect of Teriparatide on Femoral Neck Fracture Healing | |||||||||||||
Medical condition: Low trauma femoral neck fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) GR (Completed) PL (Completed) NL (Completed) DE (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: 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: 2010-021395-28 | Sponsor Protocol Number: B3D-MC-GHDN | Start Date*: 2012-04-03 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Effect of Teriparatide on Femoral Neck Fracture Healing | |||||||||||||
Medical condition: Low trauma femoral neck fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) ES (Completed) LV (Completed) FI (Completed) NO (Completed) LT (Completed) EE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
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: 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: 2004-000894-67 | Sponsor Protocol Number: B3D-MC-GHCN | Start Date*: 2004-09-01 |
Sponsor Name:Eli Lilly and Company | ||
Full Title: The Effect of Teriparatide on Distal Radius Fracture Healing | ||
Medical condition: Fracture of distal radius (Colles’) fracture | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001832-34 | Sponsor Protocol Number: 3100N7-211-WW | Start Date*: 2007-01-11 | |||||||||||
Sponsor Name:Wyeth Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Single-Blind, Randomized, Stratified, Standard-of-Care Controlled, Feasibility and Safety Study of rhBMP-2/CPM as an Adjuvant Therapy for Fractures of the Proximal Femur | |||||||||||||
Medical condition: Closed fracture of the proximal femur | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FI (Completed) HU (Completed) FR (Completed) SE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002130-20 | Sponsor Protocol Number: 1.4 | Start Date*: 2020-02-07 | ||||||||||||||||
Sponsor Name:Norfolk and Norwich University Hospitals NHS Foundation Trust | ||||||||||||||||||
Full Title: Research on Efficacy of Teriparatide use in the Return of recruits to Normal duty. | ||||||||||||||||||
Medical condition: Healthy individuals with stress fractures. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
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: 2006-005093-40 | Sponsor Protocol Number: CS I-040202/01 | Start Date*: 2007-10-22 | |||||||||||
Sponsor Name:Kuros Biosurgery AG | |||||||||||||
Full Title: A phase II randomized, controlled, open-labeled (dose-blinded) dose finding study of the safety and efficacy of I-040202 in the treatment of patients with acute open tibial shaft fractures | |||||||||||||
Medical condition: Acute open tibial shaft fractures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) HU (Completed) SI (Completed) FI (Completed) CZ (Completed) SK (Completed) IT (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
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