- Trials with a EudraCT protocol (155)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
155 result(s) found for: Femoral neck.
Displaying page 1 of 8.
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: 2014-001702-18 | 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: 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: 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: 2005-004149-33 | Sponsor Protocol Number: 05-FNF-007 | Start Date*: 2006-01-30 | |||||||||||
Sponsor Name:Stryker Biotech, LLC | |||||||||||||
Full Title: A randomized, controlled trial of the effect of Osigraft when used in the treatment of displaced femoral neck fractures – a pilot study | |||||||||||||
Medical condition: Displaced femoral neck fractures are classified as Garden III and IV according to the Garden classification system for femoral neck fractures. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001116-65 | Sponsor Protocol Number: B3D-MC-GHDQ | Start Date*: 2012-02-10 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Second study on the Effect of Teriparatide on Femoral Neck Fracture Healing | |||||||||||||
Medical condition: Low trauma femoral neck fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) GR (Completed) PL (Completed) NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021395-28 | Sponsor Protocol Number: B3D-MC-GHDN | Start Date*: 2012-04-03 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Effect of Teriparatide on Femoral Neck Fracture Healing | |||||||||||||
Medical condition: Low trauma femoral neck fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) ES (Completed) LV (Completed) FI (Completed) NO (Completed) LT (Completed) EE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003726-14 | Sponsor Protocol Number: protocol4_1tdn | Start Date*: 2015-10-12 | |||||||||||
Sponsor Name:Thomas Fichtner Bendtsen | |||||||||||||
Full Title: Gluteus medius fascia plane block - Validating a new nerve block technique | |||||||||||||
Medical condition: Hip fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007205-36 | Sponsor Protocol Number: 2008.519/20 | Start Date*: 2009-03-26 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: DETERMINATION DE LA DOSE MINIMALE EFFICACE DE ROPIVACAINE POUR RACHIANESTHÉSIE UNILATÉRALE HYPOBARE AU COURS DE LA CHIRURGIE TRAUMATIQUE DU COL FÉMORAL CHEZ LA PERSONNE ÂGÉE : ÉTUDE PROSPECTIVE COM... | |||||||||||||
Medical condition: Fracture du col du fémur | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
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: 2009-015939-33 | Sponsor Protocol Number: 20080394 | Start Date*: 2010-03-23 |
Sponsor Name:Amgen Inc | ||
Full Title: A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults with Fresh Unilateral Intertrochanteric Fracture of the P... | ||
Medical condition: Acceleration of fracture healing | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: FR (Completed) GB (Completed) DE (Completed) SE (Completed) PL (Completed) DK (Completed) NL (Completed) LV (Completed) GR (Completed) IT (Completed) HU (Completed) BE (Completed) FI (Completed) LT (Completed) EE (Completed) BG (Completed) SI (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-004119-19 | Sponsor Protocol Number: 2015-005-M | Start Date*: 2016-04-25 |
Sponsor Name:Reinier de Graaf Hospital | ||
Full Title: Femoral Nerve Blockage in Proximal Femoral Fractures in patients of 65 years of age or older, a Randomised Controlled Trial | ||
Medical condition: Pain in patients with a proximal femoral fracture. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013134-24 | Sponsor Protocol Number: RGHT000675 | Start Date*: 2009-07-31 |
Sponsor Name:Belfast Health & Social Care Trust | ||
Full Title: Comparison of fascia iliaca compartment block or femoral nerve block using levobupivacaine for postoperative analgesia after operative repair of femoral neck fracture: a dose response study | ||
Medical condition: Postoperative Analgesia in patients undergoing operative repair of fractured neck of femur | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-005529-37 | Sponsor Protocol Number: 07.12.2015 | Start Date*: 2016-02-29 | |||||||||||
Sponsor Name:Bente Lomholt Langdahl | |||||||||||||
Full Title: Treatment with zoledronic acid subsequent to denosumab in osteoporosis | |||||||||||||
Medical condition: Osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000931-18 | Sponsor Protocol Number: EL-THOS-001 | Start Date*: 2014-05-27 |
Sponsor Name:Ersi Voskaridou-Dimoula | ||
Full Title: EVALUATION OF EFFICACY OF DENOSUMAB IN PATIENTS WITH THALASSEMIA MAJOR AND OSTEOPOROSIS: A RANDOMIZED, PLACEBO-CONTROLLED, SINGLE-SITE, DOUBLE BLIND PHASE 2B CLINICAL TRIAL | ||
Medical condition: Adult patients with Thalassemia major and osteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
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: 2006-006692-20 | Sponsor Protocol Number: independant Trial (TOMIBA-TRIAL01) | Start Date*: 2007-09-06 |
Sponsor Name:St. Vincent Hospital, Medical Department II | ||
Full Title: The TOMIBA study Treatment of Osteoporotic Men With Intravenous Ibandronate An open-label, single-center, prospective Phase III study | ||
Medical condition: Osteoporosis in Men | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
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: 2007-002693-66 | Sponsor Protocol Number: 0822-018 | Start Date*: 2007-11-13 | |||||||||||
Sponsor Name:MERCK SHARP & DOHME CORP. | |||||||||||||
Full Title: A Phase III Randomized, Placebo-Controlled Clinical Trial to Assess the Safety and Efficacy of MK-0822 to Reduce the Risk of Fracture in Osteoporotic Postmenopausal Women Treated With Vitamin D an... | |||||||||||||
Medical condition: Postmenopausal Osteoporosis | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: LT (Completed) DK (Completed) CZ (Prematurely Ended) PL (Prematurely Ended) GB (Prematurely Ended) DE (Completed) FR (Prematurely Ended) BE (Prematurely Ended) LV (Completed) EE (Completed) IT (Completed) ES (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005551-32 | Sponsor Protocol Number: 20110174 | Start Date*: 2014-06-16 | |||||||||||
Sponsor Name:Amgen, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double blind, Placebo controlled Study to Compare the Efficacy and Safety of Romosozumab With Placebo in Men With Osteoporosis | |||||||||||||
Medical condition: male osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) BE (Completed) DK (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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