- Trials with a EudraCT protocol (149)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
149 result(s) found for: Hip fracture.
Displaying page 2 of 8.
EudraCT Number: 2016-000377-20 | Sponsor Protocol Number: VK5211-201 | Start Date*: 2016-05-27 | |||||||||||
Sponsor Name:Viking Therapeutics, Inc. | |||||||||||||
Full Title: A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects with Acute Hip Fracture | |||||||||||||
Medical condition: Hip fracture | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000078-36 | Sponsor Protocol Number: protocol2tdn | Start Date*: 2015-03-17 | |||||||||||
Sponsor Name:Thomas Fichtner Bendtsen | |||||||||||||
Full Title: Analgetisk effekt af proksimal supplerende nervus obturatorius blokade efter insufficient analgetisk effekt af nervus femoralis blokade hos patienter med hoftenær femurfraktur | |||||||||||||
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: 2014-001923-53 | Sponsor Protocol Number: 7980 | Start Date*: 2015-10-07 | |||||||||||
Sponsor Name:Rafael Bielza Galindo | |||||||||||||
Full Title: Intravenous iron, early functional recovery and delirium in patients atients with hip fracture | |||||||||||||
Medical condition: Hip fracture | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003875-77 | Sponsor Protocol Number: 1870 | Start Date*: 2018-01-24 | |||||||||||
Sponsor Name:University Hospitals of North Midlands NHS Trust | |||||||||||||
Full Title: A Randomised, Controlled Double Blinded Non-inferiority Trial of intravenous Morphine compared with intravenous Paracetamol for pain relief in patients presenting to the Emergency Department with S... | |||||||||||||
Medical condition: Fractured Neck of Femur | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003326-27 | Sponsor Protocol Number: NAROP11 | Start Date*: 2011-12-05 |
Sponsor Name:Landstinget i Värmland | ||
Full Title: Is regional anaethesia of the hip preferable over traditional analgesia in the acute stage of the management of patients with a fracture of the hip? | ||
Medical condition: fracture of the hip | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
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: 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: 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: 2007-001048-32 | Sponsor Protocol Number: 0701017 | Start Date*: 2008-09-15 | |||||||||||||||||||||||||||||||
Sponsor Name:CHU SAINT-ETIENNE | |||||||||||||||||||||||||||||||||
Full Title: Prospective, multicentre, open-label study evaluating Fondaparinux (1,5 mg/day) in venous thromboembolic events prevention in patients with renal impairment defined by a creatinin clearance between... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with renal impairment defined by a creatinin clearance between 20 and 50 ml/min and undergoing a major orthopaedic surgery (hip fracture, total hip replacement and total knee replacement) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||||||||||||
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: 2017-001778-40 | Sponsor Protocol Number: VITAMINA_D | Start Date*: 2017-10-11 |
Sponsor Name:Leonor Cuadra Llopart | ||
Full Title: A Prospective Randomized Trial Comparing the Effect of 2 vitamin D supplementation regimens in elderly people after hip fracture surgery | ||
Medical condition: Hip fracture and vitamin D deficiency | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004986-41 | Sponsor Protocol Number: IC4-12911-098-CZE | Start Date*: 2005-12-09 | |||||||||||
Sponsor Name:Servier s.r.o | |||||||||||||
Full Title: PRotelos 2g in the OSteoporosis treatment, the Tolerability and Efficacy Profile | |||||||||||||
Medical condition: Treatment of postmenopausal osteoporosis to reduce the risk of hip and vertebral fractures [Osteoporotic fracture] | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
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: 2016-001108-47 | Sponsor Protocol Number: BARIFER | Start Date*: 2016-05-29 |
Sponsor Name:Fundació Hospital Universitari Vall Hebron-Institut de Recerca (VHIR) | ||
Full Title: Impact of eradication of asymptomatic bacteriuria on reducing the incidence of early infection in patients with periprosthetic femoral fractures requiring hip hemiarthroplasty | ||
Medical condition: Early infection in patients with periprosthetic femoral fracture | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004250-15 | Sponsor Protocol Number: | Start Date*: 2018-06-08 | |||||||||||
Sponsor Name:University Hospitals Birmingham | |||||||||||||
Full Title: A prospective, phase II, single centre, cross-sectional, randomised trial investigating Dehydroepiandrosterone and it's Pharmacokinetics in Trauma | |||||||||||||
Medical condition: DHEA depletion in trauma and hip fracture patients. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003850-10 | Sponsor Protocol Number: Laxatives26092019 | Start Date*: 2020-02-10 | |||||||||||
Sponsor Name:Hospital Pharmacy Funen, Research Department, Odense University Hospital | |||||||||||||
Full Title: Oral laxatives after hip fracture surgery: A randomised controlled trial. | |||||||||||||
Medical condition: The aim is to investigate which constipation therapy is the most optimal choice for postoperative treatment in older patients after hip fracture surgery. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
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 (Completed) | |||||||||||||
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: 2008-002693-35 | Sponsor Protocol Number: B3D-EW-GHDK | Start Date*: 2008-11-21 | |||||||||||
Sponsor Name:Eli Lilly and Company Ltd | |||||||||||||
Full Title: Comparison of the Effects of Teriparatide with those of Risedronate on Lumbar Spine Bone Mineral Density in Men and Postmenopausal Women with Low Bone Mass and a Recent Pertrochanteric Hip Fracture | |||||||||||||
Medical condition: Postmenopausal Women and Men with Low Bone Mass and a Recent Pertrochanteric Fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) DE (Completed) GB (Completed) ES (Completed) IT (Completed) GR (Completed) SE (Completed) AT (Completed) FR (Completed) CZ (Completed) IE (Completed) FI (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002732-22 | Sponsor Protocol Number: CL3-12911-019 | Start Date*: 2006-09-08 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: A double-blind, multicentric, multinational randomised study to assess the effects of two years administration of 2g per day of strontium ranelate versus alendronate 70mg per week in women with pos... | |||||||||||||
Medical condition: Treatment of postmenopausal Osteoporosis to reduce the risk of hip and vertebral fractures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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