- 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 6 of 8.
EudraCT Number: 2004-002317-37 | Sponsor Protocol Number: HMR4003B/4034 | Start Date*: 2004-11-18 | |||||||||||
Sponsor Name:Aventis Inc. | |||||||||||||
Full Title: OPEN-LABEL STUDY TO DETERMINE HOW PRIOR THERAPY WITH ALENDRONATE OR RISEDRONATE IN POSTMENOPAUSAL WOMEN WITH OSTEOPOROSIS INFLUENCES THE CLINICAL EFFECTIVENESS OF TERIPARATIDE | |||||||||||||
Medical condition: Post-menopausal woman with 1 or more prevalent osteoporotic fractures and a BMD (spine or hip) of < -2.5 (see protocol amendment 2). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001153-17 | Sponsor Protocol Number: 262 | Start Date*: 2008-06-16 | |||||||||||
Sponsor Name:MSD | |||||||||||||
Full Title: Phase III (Phase V Program), Open-Label, Randomized, Referred- Care-Controlled, Clinical Trial to Evaluate the Efficacy and Safety of MK-0217A/Alendronate Sodium 70 mg/Vitamin D3 5600 I.U. Combinat... | |||||||||||||
Medical condition: Postmenopausal women with osteoporosis at increased risk of falls. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) ES (Completed) LT (Completed) GB (Completed) BE (Completed) LV (Completed) FR (Completed) IE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006015-72 | Sponsor Protocol Number: CR9108963 | Start Date*: 2007-08-10 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd. | |||||||||||||
Full Title: Study CR9108963: A 12-month, randomized, double blind, parallel-group, placebo and active-controlled dose-range finding study of the efficacy and safety of SB-751689 in post-menopausal women with o... | |||||||||||||
Medical condition: Post-menopausal Osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) DK (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004807-11 | Sponsor Protocol Number: BA058-05-021 | Start Date*: 2020-04-27 | |||||||||||
Sponsor Name:Radius Health Inc. | |||||||||||||
Full Title: A Randomized, Non-Inferiority, Phase 3, Open-Label, Multicenter Study to Evaluate the Efficacy and Safety of Abaloparatide-sMTS for the Treatment of Postmenopausal Women with Osteoporosis | |||||||||||||
Medical condition: Osteoporosis in postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) DK (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002390-13 | Sponsor Protocol Number: notapplicable | Start Date*: 2009-04-08 | |||||||||||
Sponsor Name:University Hospital | |||||||||||||
Full Title: Are cranberry capsules useful in preventing urinary tract infection in hip fracture patients with urinary tract catheter | |||||||||||||
Medical condition: Urinary tract infections in patients with hip fractures. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015058-38 | Sponsor Protocol Number: OR09/9018 | Start Date*: 2010-10-22 |
Sponsor Name:University of Leeds | ||
Full Title: Improving the outcome for patients after osteoporotic femoral fractures | ||
Medical condition: OSTEOPOROTIC FEMORAL FRACTURE | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-012926-35 | Sponsor Protocol Number: 5442-001-02 | Start Date*: 2009-09-28 | |||||||||||
Sponsor Name:Merck & Co, Inc. | |||||||||||||
Full Title: A Phase IIb, Randomized, Placebo-Controlled, Dose-Ranging Study of MK-5442 in the Treatment of Postmenopausal Women with Osteoporosis | |||||||||||||
Medical condition: Osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000663-45 | Sponsor Protocol Number: PREVENT-iT-2021.07 | Start Date*: 2023-02-01 |
Sponsor Name:Hamilton Health Sciences Corporation | ||
Full Title: Prospective Randomized Evaluation of Emerging Novel Treatments for Infection prophylaxis in Total Joint Replacement (PREVENT-iT): A Pilot Study | ||
Medical condition: Persistent Draining Wound and Periprosthetic Joint Infection prevention in patients undergoing total joint replacement | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000852-91 | Sponsor Protocol Number: W15.032 | Start Date*: 2016-06-02 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Zoledronic Acid to Maintain Bone Mass After Denosumab Discontinuation: AfterDmab | |||||||||||||
Medical condition: Treatment of patients with with postmenopausal osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002174-30 | Sponsor Protocol Number: B3D-US-GHCV | Start Date*: 2005-09-09 |
Sponsor Name:Eli Lilly and Company | ||
Full Title: The Use of Nuclear Scintigraphy to Evaluate the Anabolic Effects of Teriparatide on the Skeleton in Postmenopausal Women in Osteoporosis | ||
Medical condition: Oesteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-000811-24 | Sponsor Protocol Number: 308260 | Start Date*: 2004-11-19 | |||||||||||
Sponsor Name:Schering AG | |||||||||||||
Full Title: Multicenter, double-blind, randomized, pleacebo-controlled study to evaluate the oral low-dose estradiol preparations SH T 04170 E (100 µg estradiol) and SH T 04170 F (190 µg estradiol) in postmeno... | |||||||||||||
Medical condition: postmenopausal women with high risk for osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010205-37 | Sponsor Protocol Number: 20080098 | Start Date*: 2009-10-28 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo Controlled Study to Compare the Efficacy and Safety of Denosumab versus Placebo in Males with Low Bone Mineral Density | |||||||||||||
Medical condition: Male Osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) FR (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000447-40 | Sponsor Protocol Number: FARM12FEXH(TESS) | Start Date*: 2017-07-12 | ||||||||||||||||
Sponsor Name:ASST SANTI PAOLO E CARLO | ||||||||||||||||||
Full Title: IMPACT ON BONE MINERAL DENSITY (BMD) OF TDF-SPARING ANTIRETROVIRAL REGIMENS IN HIV-POSITIVE MENOPAUSAL WOMEN AFFECTED BY OSTEOPENIA: THE TENOFOVIR SPARING STRATEGY (TESS) STUDY | ||||||||||||||||||
Medical condition: HIV-positive women affected by osteopenia. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003888-56 | Sponsor Protocol Number: 20192022 | Start Date*: 2021-01-30 | |||||||||||
Sponsor Name:Department of Nephrology, Herlev & Gentofte Hospital, Herlev Hospital | |||||||||||||
Full Title: Treatment of adynamic bone disorder with parathyroid hormone in patients with chronic kidney disease | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007456-34 | Sponsor Protocol Number: 3100N0-2213-WW | Start Date*: 2009-09-04 | ||||||||||||||||
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc | ||||||||||||||||||
Full Title: Estudio de fase 2, multicéntrico, aleatorizado, controlado con producto activo, de grupos paralelos, búsqueda de dosis y de la seguridad de la proteína morfogenética de hueso humano recombinante 2 ... | ||||||||||||||||||
Medical condition: Sujetos con disminución de la densidad mineral ósea (DMO) en riesgo de fractura de cadera | ||||||||||||||||||
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Population Age: Elderly | Gender: Female | |||||||||||||||||
Trial protocol: ES (Completed) BE (Completed) PL (Completed) FI (Prematurely Ended) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020040-35 | Sponsor Protocol Number: CL0002 | Start Date*: 2010-10-21 | ||||||||||||||||
Sponsor Name:MicroCHIPS | ||||||||||||||||||
Full Title: Pharmacokinetics of hPTH (1-34) delivery with MicroCHIPS’ implantable reservoir array device. | ||||||||||||||||||
Medical condition: Osteoporosis Osteopenia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014729-18 | Sponsor Protocol Number: 5442-012-00 | Start Date*: 2009-11-30 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: Un Ensayo de Fase IIb, Aleatorizado, Doble Ciego, Controlado con Placebo y Comparador Activo, de Determinación del Rango de Dosis para Evaluar los Efectos de MK-5442 en la Densidad Mineral Ósea ... | |||||||||||||
Medical condition: Osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) GB (Completed) CZ (Completed) DK (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-006017-38 | Sponsor Protocol Number: RGB-14-101 | Start Date*: 2021-07-13 | |||||||||||
Sponsor Name:Gedeon Richter Plc. | |||||||||||||
Full Title: A Randomised, Double-blind, Multicentre Phase III Study to Assess the Efficacy and Safety of RGB-14-P Compared to Prolia® in Women with Postmenopausal Osteoporosis | |||||||||||||
Medical condition: Postmenopausal osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: PL (Completed) CZ (Completed) HU (Completed) BG (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003138-16 | Sponsor Protocol Number: Ed001 | Start Date*: 2005-08-26 | |||||||||||
Sponsor Name:R+ D department, Hull and East Yorkshire NHS Hospital Trust | |||||||||||||
Full Title: A clinical observational study to assess the effectiveness of Strontium Ranelate on bone protection in osteoporotic patients pre-treated with bisphosphonates. | |||||||||||||
Medical condition: Postmenopausal Osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004303-59 | Sponsor Protocol Number: NAROP08 | Start Date*: 2008-10-24 |
Sponsor Name:Örebro Läns Landsting | ||
Full Title: Blockad av femoralnerven till patienter med misstänkt höftfraktur – fungerar den i klinisk praxis? Eng: Blocking the femoral nerve on patients with suspected hip fracture - does it work in clinica... | ||
Medical condition: misstänkt höftfraktur | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
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