- Trials with a EudraCT protocol (52)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
52 result(s) found for: Fracture reduction.
Displaying page 1 of 3.
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: 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: 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: 2006-003688-30 | 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: 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: 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: 2022-003163-21 | Sponsor Protocol Number: COTHUGMTRA22 | Start Date*: 2023-07-13 | |||||||||||
Sponsor Name:Coral Sánchez Pérez | |||||||||||||
Full Title: PHASE III, SINGLE-CENTER, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, LOW-INTERVENTION CLINICAL TRIAL IN TWO PARALLEL GROUPS, TO EVALUATE EFFICACY AND SAFETY IN ELDERLY PATIENTS WITH PERTROCHANTE... | |||||||||||||
Medical condition: pertrochanteric hip fracture | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
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) |
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) |
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: 2022-001857-22 | Sponsor Protocol Number: Methadone-010922 | Start Date*: 2022-09-06 | |||||||||||||||||||||||||||||||
Sponsor Name:Sygehus Sønderjylland, Orthopedic department | |||||||||||||||||||||||||||||||||
Full Title: Perioperative Methadone for ameliorating postoperative pain and reduction in postoperative opioid consumption in hip fracture patients – Dosage adjusting pilot-study | |||||||||||||||||||||||||||||||||
Medical condition: Hip fractures | |||||||||||||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001702-18 | Sponsor Protocol Number: protocol1tdn | Start Date*: 2014-08-28 | |||||||||||
Sponsor Name:Thomas Fichtner Bendtsen | |||||||||||||
Full Title: Analgesic duration of a preoperative single-shot femoral nerve block with Bupivacaine and adjuvant Dexamethasone in patients with hip fracture | |||||||||||||
Medical condition: Pain in patients with hip fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003643-38 | Sponsor Protocol Number: 17-HPNCL-01 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Fondation Lenval - Hôpitaux Pédiatriques de Nice CHU-LENVAL | |||||||||||||
Full Title: INTRANASAL KETAMINE IN THE REDUCTION OF THE ISOLATED FRACTURES OF THE HIGHER MEMBER OF THE CHILD TO PEDIATRIC EMERGENCIES | |||||||||||||
Medical condition: a fracture isolated from the distal end of the closed upper limb, requiring a reduction | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022587-12 | Sponsor Protocol Number: VitK | Start Date*: 2015-01-20 | ||||||||||||||||||||||||||
Sponsor Name:Guy's and St. Thomas' NHS Foundation Trust | ||||||||||||||||||||||||||||
Full Title: The Additive effect of Vitamin K Supplementation and Bisphosphonate on Fracture Risk in Post-menopausal Osteoporosis | ||||||||||||||||||||||||||||
Medical condition: Post-menopausal osteoporosis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000528-32 | Sponsor Protocol Number: TRaffiq | Start Date*: 2018-07-12 | |||||||||||
Sponsor Name:Consorci Mar Parc de Salut de Barcelona (Parc de Salut Mar) | |||||||||||||
Full Title: Tranexamic acid use to reduce de blood transfusion in femur fracture patients. Clinical randomized trial with placebo control | |||||||||||||
Medical condition: Bleeding in patients suffering femur neck fracture | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002304-89 | Sponsor Protocol Number: protocol2_2tdn | Start Date*: 2015-07-30 | |||||||||||
Sponsor Name:Thomas Fichtner Bendtsen | |||||||||||||
Full Title: Preoperative analgesic affect of combined obturator and femoral nerve block compared to femoral nerve block alone, in patients with hip fracture. | |||||||||||||
Medical condition: Hip fracture | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
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: 2010-020973-18 | Sponsor Protocol Number: L00006CP405 | Start Date*: 2011-03-01 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: “Effect of treatment with ossein-hydroxyapatite compound on the time of fracture-healing”. A prospective, multicenter, double-blind, randomised, placebo controlled clinical trial. | |||||||||||||
Medical condition: Wrist fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
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