- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
22 result(s) found for: Broken Hip.
Displaying page 1 of 2.
| 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: 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: 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: 2009-017153-35 | Sponsor Protocol Number: ALMED-08-C2-020 | Start Date*: 2010-04-06 | |||||||||||
| Sponsor Name:AIR LIQUIDE SANTE INTERNATIONAL | |||||||||||||
| Full Title: An international, multi-center, randomized, controlled trial evaluating the effect of xenon on post-operative delirium in elderly patients undergoing hip fracture surgery. | |||||||||||||
| Medical condition: Post-operative delirium after hip fracture surgery under general anaesthesia | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) GB (Completed) ES (Completed) IT (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004697-21 | Sponsor Protocol Number: PENG-CAD | Start Date*: 2020-12-11 | |||||||||||
| Sponsor Name:Instituto de Investigación Biomédica de Salamanca | |||||||||||||
| Full Title: RANDOMIZED AND CONTROLLED PHASE IV CLINICAL TRIAL ON THE ANALGESIC EFFECTIVENESS OF THE COMBINED BLOCKADE (PENG -PERICAPSULAR NERVE GROUP- AND THE FEMORAL LATERAL CUTANEOUS NERVE) IN THE HIP FRACTU... | |||||||||||||
| Medical condition: Most appropriate anesthetic technique for surgery of hip fracture in the elderly | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002354-20 | Sponsor Protocol Number: VIK_001 | Start Date*: 2016-09-14 | |||||||||||
| Sponsor Name:DOTT.SSA CARMELINDA RUGGIERO,ISTITUTO DI GERIATRIA E GERONTOLOGIA, UNIVERSITà DEGLI STUDI DI PERUGIA | |||||||||||||
| Full Title: EFFECTIVNESS OF WARFARIN REVERSAL USING INTRAVENOUS VITAMIN K AMONG HIP FRACTURE OLDER PERSONS: A RANDOMIZED CLINICAL TRIAL | |||||||||||||
| Medical condition: Hip fractured subjects on warfarin therapy | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| 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: 2010-023871-25 | Sponsor Protocol Number: 2010-023871-25 | Start Date*: 2011-04-20 | |||||||||||||||||||||
| Sponsor Name:Nottingham University Hospitals NHS Trust | |||||||||||||||||||||||
| Full Title: The FINOF(Femoral Nerve-Block Intervention in Neck Of Femur Fracture) Study | |||||||||||||||||||||||
| Medical condition: Pain and mobility following hip fracture in the elderly | |||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2009-015865-30 | Sponsor Protocol Number: PAHFRAC-01 | Start Date*: 2010-06-24 | |||||||||||
| Sponsor Name:Máximo Bernabeu Wittel | |||||||||||||
| Full Title: ENSAYO CLINICO RANDOMIZADO DOBLE CIEGO DE HIERRO CARBOXIMALTOSA INTRAVENOSO CON O SIN ERITOPOYETINA PARA LA PREVENCIÓN DE TRANSFUSIONES DE CONCENTRADOS DE HEMATÍES EN EL PERIOPERATORIO DE FRACTURA ... | |||||||||||||
| Medical condition: Pacientes adultos ingresados en el Hospital por fractura de cadera osteoporótica. Adult patients admitted in Hospital for osteoporotic hip fracture | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022816-38 | Sponsor Protocol Number: 2010-09-20 | Start Date*: 2010-12-22 | ||||||||||||||||
| Sponsor Name:Department of Anesthesiology & Intensive Care | ||||||||||||||||||
| Full Title: Preoperative Optimization of the High-Risk Patient undergoing Hip Fracture Surgery | ||||||||||||||||||
| Medical condition: Patients with elevated NT-proBNP as a sign of left ventricular dysfunction undergoing hipfracturesurgery. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| 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: 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: 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: 2013-003439-31 | Sponsor Protocol Number: CBYM338D2201 | Start Date*: 2014-06-17 | ||||||||||||||||
| Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
| Full Title: A 24-week Double-blind Treatment and 24-week Follow-up, Randomized, Multicenter, Placebo-controlled, Phase IIa/IIb Study to Evaluate Safety and Efficacy of i.v. Bimagrumab on Total Lean Body Mass a... | ||||||||||||||||||
| Medical condition: Patients with muscle wasting (atrophy) after hip fracture surgery and subsequent postsurgical rehabilitation | ||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) GB (Completed) DE (Completed) HU (Completed) CZ (Completed) AT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| 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: 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: 2011-003233-34 | Sponsor Protocol Number: 11048 | Start Date*: 2012-01-19 |
| Sponsor Name:University of Nottingham | ||
| Full Title: The effect of intravenous iron on postoperative transfusion requirements in hip fracture patients – a pilot study | ||
| Medical condition: Anaemia following hip fracture | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-013462-25 | Sponsor Protocol Number: MW001 | Start Date*: 2009-09-28 | |||||||||||
| Sponsor Name:NHS Greater Glasgow and Clyde Health Board | |||||||||||||
| Full Title: A dose finding study for ultrasound guided anterior psoas compartment blocks in patients with a fractured neck of femur | |||||||||||||
| Medical condition: Proximal traumatic fractured neck of femur | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021263-33 | Sponsor Protocol Number: 3001101 | Start Date*: 2011-05-24 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Sykehuset i Vestfold HF | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: PERIOPERATIVE LEVOSIMENDAN INFUSION IN PATIENTS WITH HEART FAILURE UNDERGOING NON-CARDIAC SURGERY: A PROSPECTIVE, RANDOMISED, PLACEBO-CONTROLLED, DOUBLE-BLIND, MULTICENTER STUDY | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Patients with serious cardiac failure scheduled for non-cardiac surgery | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-004698-42 | Sponsor Protocol Number: 10102016 | Start Date*: 2017-05-29 |
| Sponsor Name: | ||
| Full Title: MORphine use in the Fascia Iliaca Compartment block with UltraSound guidance. | ||
| Medical condition: Pain in proximal femur fractures | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
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