- Trials with a EudraCT protocol (149)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
149 result(s) found for: Hip fracture.
Displaying page 4 of 8.
EudraCT Number: 2004-000512-17 | Sponsor Protocol Number: 20040138 | Start Date*: 2004-10-01 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-controlled Study to Evaluate AMG 162 in the Treatment of Bone Loss in Subjects Undergoing Androgen-Deprivation Therapy for Non-metastatic Prostate Cancer | |||||||||||||
Medical condition: Bone loss in pateints undergoing androgen-deprivation therapy (ADT) for non-metastatic prostate cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) HU (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004001-26 | Sponsor Protocol Number: 06AE001 | Start Date*: 2007-02-23 | |||||||||||
Sponsor Name:Nottingham University Hospitals NHS Trust | |||||||||||||
Full Title: A Randomised Controlled Trial of Fascia Iliaca Compartment Block vs. Morphine For Pain in Fractured Neck of Femur in the Emergency Department: A Pilot Study | |||||||||||||
Medical condition: Suspected isolated hip fracture - Clinical suspicion of hip fracture is defined as the presence of painful, unilateral shortening and external rotation of the lower limb preventing weight-bearing. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011920-69 | Sponsor Protocol Number: 0822-043-00 | Start Date*: 2011-08-05 |
Sponsor Name:Merck & Co., Inc. | ||
Full Title: A Quantitative Computed Tomography (QCT) Sub-Study of the Phase III Randomized, Placebo-Controlled Clinical Trial to Assess the Safety and Efficacy of Odanacatib (MK-0822) to Reduce the Risk of Fra... | ||
Medical condition: postmenopausal osteoporosis | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: NO (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-004131-57 | Sponsor Protocol Number: CZOL446M2309 | Start Date*: 2007-04-13 | |||||||||||
Sponsor Name:Novartis Pharma Services AG [...] | |||||||||||||
Full Title: A two year multicenter, randomized, double-blind, placebo-controlled, parallel group study to evaluate the fracture efficacy and safety of intravenous zoledronic acid 5 mg annually for the treatmen... | |||||||||||||
Medical condition: Treatment of osteoporosis in men | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) BE (Completed) CZ (Completed) HU (Completed) DE (Completed) PT (Completed) SK (Completed) GB (Completed) IT (Completed) PL (Completed) AT (Completed) IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007947-28 | Sponsor Protocol Number: EFC10636 | Start Date*: 2008-08-27 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: A Multinational, Multicenter, Randomized, Double-Blind study Comparing the Efficacy and Safety of AVE5026 with placebo for the Extended Prevention of Venous Thromboembolism in Patients Having Under... | |||||||||||||
Medical condition: The subjects who will participate to this clinical trial are patients having undergone hip fracture surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (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: 2010-019454-41 | Sponsor Protocol Number: 0822-053 | Start Date*: 2010-07-16 | |||||||||||
Sponsor Name:Merck Sharp & Dohm Corp. | |||||||||||||
Full Title: A Phase III Randomized, Placebo-Controlled Clinical Trial to Assess the Safety and Efficacy of Odanacatib (MK-0822) in the treatment of Men with Osteoporosis Treated with Vitamin D and Calcium | |||||||||||||
Medical condition: osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: LV (Completed) DK (Completed) GB (Completed) NL (Completed) EE (Completed) IT (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002188-31 | Sponsor Protocol Number: HLX14-002-PMOP301 | Start Date*: 2022-11-25 | |||||||||||
Sponsor Name:Shanghai Henlius Biotech, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, International Multicenter, Parallel-Controlled Phase III Clinical Study to Evaluate Recombinant Anti-RANKL Human Monoclonal Antibody Injection (HLX14) Versus Denosumab I... | |||||||||||||
Medical condition: Osteoporosis at High Risk of Fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002511-83 | Sponsor Protocol Number: TTP889-201 | Start Date*: 2005-01-03 | |||||||||||
Sponsor Name:TransTech Pharma | |||||||||||||
Full Title: A Multi-Center, Placebo-Controlled Evaluation of the Safety and Efficacy of Three Weeks Extended VTE Prophylaxis with Daily Oral Doses of TTP889 After One Week of Standard Prophylactic Treatment Fo... | |||||||||||||
Medical condition: Antithrombotic in patients at risk for venous thromboembolism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) CZ (Completed) SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001201-27 | Sponsor Protocol Number: P07038 | Start Date*: 2011-11-07 |
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., USA | ||
Full Title: A randomized, controlled, parallel-group, double-blind trial of sugammadex or usual care (neostigmine or spontaneous recovery) for reversal of rocuronium- or vecuronium-induced neuromuscular blocka... | ||
Medical condition: not applicable | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) BE (Completed) NL (Prematurely Ended) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-000138-35 | Sponsor Protocol Number: 20030216 | Start Date*: 2004-08-12 |
Sponsor Name:Amgen Inc | ||
Full Title: A Study to Evaluate AMG 162 in the Treatment of Postmenopausal Osteoporosis FREEDOM (Fracture REduction Evaluation of Denosumab in Osteoporosis every & Months) | ||
Medical condition: Treatment of postmenopausal osteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Completed) FI (Completed) LV (Completed) NO (Completed) SK (Completed) ES (Completed) AT (Completed) LT (Completed) CZ (Completed) HU (Completed) GB (Completed) DK (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-001702-15 | Sponsor Protocol Number: R475-OA-1688 | Start Date*: 2018-03-05 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase 3 Randomized, Double-Blind, Multi-Dose, Placebo And NSAID-Controlled Study To Evaluate The Efficacy And Safety Of Fasinumab In Patients With Pain Due To Osteoarthritis Of The Knee Or Hip | ||||||||||||||||||
Medical condition: Pain due to osteoarthritis of the knee or hip | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) DE (Completed) EE (Completed) GB (GB - no longer in EU/EEA) RO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003359-39 | Sponsor Protocol Number: ZEST | Start Date*: 2014-01-14 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
Full Title: Bisphosphonate Therapy with Zoledronic acid or Tenofovir Switching to Improve Low Bone Mineral Density in HIV-Infected Adults | |||||||||||||
Medical condition: low bone mineral density - HIV | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005258-29 | Sponsor Protocol Number: B3D-MC-GHCY | Start Date*: 2006-04-12 |
Sponsor Name:Eli Lilly and Company Limited | ||
Full Title: The Effect of Teriparatide Compared with Risedronate on Back Pain in Postmenopausal Women with Osteoporotic Vertebral Fractures | ||
Medical condition: chronic back pain and osteoporotic vertebral fracture(s) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) ES (Completed) IT (Completed) BE (Completed) SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002811-27 | Sponsor Protocol Number: OI-2011 | Start Date*: 2011-11-07 |
Sponsor Name:Bente Langdahl, consultant, ass. professor, PhD, DMSc | ||
Full Title: The Effect of Treatment with PTH and Zoledronic acid in Patients with Osteogenesis Imperfecta | ||
Medical condition: Osteogenesis imperfecta | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-002948-24 | Sponsor Protocol Number: 20080289 | Start Date*: 2013-04-08 | |||||||||||
Sponsor Name:Amgen, Inc. | |||||||||||||
Full Title: An Open-label, Randomized, Teriparatide-controlled Study to Evaluate the Effect of Treatment with AMG 785 in Postmenopausal Women with Osteoporosis Previously Treated with Bisphosphonate Therapy | |||||||||||||
Medical condition: Post Menopausal Osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) DK (Completed) ES (Completed) GB (Completed) CZ (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005275-15 | Sponsor Protocol Number: 20050209 | Start Date*: 2006-07-11 | ||||||||||||||||
Sponsor Name:Amgen Limited | ||||||||||||||||||
Full Title: A Randomized, Double- Blind, Placebo- Controlled, Multi- Center Phase 3 Study to Determine the Treatment Effect of Denosumab in Subjects with Non- Metastatic Breast Cancer Receiving Aromatase Inhib... | ||||||||||||||||||
Medical condition: Early non-metastatic breast cancer and therapy-induced bone loss and fractures | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: AT (Completed) SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004921-33 | Sponsor Protocol Number: R475-OA-1758 | Start Date*: 2018-11-09 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Effects of Fasinumab on Peripheral Nerve Function in Patients with Pain Due to Osteoarthritis of the Hip or Knee | ||||||||||||||||||
Medical condition: Pain due to osteoarthritis of the hip or knee | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-007945-11 | Sponsor Protocol Number: EFC10343 | Start Date*: 2008-05-09 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: A Multinational, Multicenter, Randomized, Double-Blind study Comparing the Efficacy and Safety of AVE5026 with enoxaparin for the Prevention of Venous Thromboembolism in Patients Undergoing Hip Fra... | |||||||||||||
Medical condition: The subjects who will participate to this clinical trial are patients undergoing Hip Fracture Surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) ES (Completed) PT (Completed) IT (Completed) CZ (Completed) GR (Completed) BG (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003087-40 | Sponsor Protocol Number: PHRC-N-2015 | Start Date*: 2017-01-17 |
Sponsor Name:UHangers | ||
Full Title: Interest of intraveinous iron and tranexamic acid to reduce transfusion in hip fracture patients - HIFIT Study | ||
Medical condition: Hip fracture | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
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