- Trials with a EudraCT protocol (153)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
153 result(s) found for: Hip replacement.
Displaying page 1 of 8.
EudraCT Number: 2008-005471-10 | Sponsor Protocol Number: 4745 | Start Date*: 2009-06-17 | |||||||||||
Sponsor Name:Nina Olofsson | |||||||||||||
Full Title: Plasma concentration of Ropivacain and Ketorolac after local infiltration during surgery in hip replacement during the first 24 postoperative hours. | |||||||||||||
Medical condition: Postoperative pain after surgery for hip replacement. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000107-94 | Sponsor Protocol Number: RB15.005 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:CHRU de Brest | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003730-10 | Sponsor Protocol Number: 001-2014-KHTY | Start Date*: 2014-12-01 | ||||||||||||||||
Sponsor Name:Department of Anesthesiology, Næstved Hospital | ||||||||||||||||||
Full Title: Effect of a lateral nerve of the thigh block on post-operative pain among patients with pain (VAS>40mm) during flexion of the hip the first or second postoperative day | ||||||||||||||||||
Medical condition: Pain after total hip replacement surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000628-14 | Sponsor Protocol Number: ISS20109714 | Start Date*: 2013-09-13 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Denosumab in enhancement of bone bonding of hip prosthesis in postmenopausal women: a randomized, double-blind, placebo-controlled study | |||||||||||||
Medical condition: Hip osteoarthritis | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000926-21 | Sponsor Protocol Number: AMSC-BDT-002 | Start Date*: 2016-10-06 | |||||||||||
Sponsor Name:Fakultní nemocnice Hradec Králové | |||||||||||||
Full Title: Innovation of method cryopreservation for clinical use autologous multipotent mesenchymal stem cells (MSCs) for treatment of extensive skeletal defects in revision surgery of total hip arthroplasty+ | |||||||||||||
Medical condition: Revision total hip arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002122-12 | Sponsor Protocol Number: FICB2014 | Start Date*: 2014-07-17 | |||||||||||
Sponsor Name:az turnhout | |||||||||||||
Full Title: Longitudinal Fascia Iliaca Compartment Block for Total Hip Arthroplasty | |||||||||||||
Medical condition: Our hypothesis is that a longitudinal approach to the fascia iliaca with a larger volume of local anesthetic will decrease morphine consumption and pain scores in patients after total hip arthropla... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000068-14 | Sponsor Protocol Number: HIP/FUSION#2 | Start Date*: 2017-05-24 | |||||||||||
Sponsor Name:Institut for Klinisk Medicin, Aarhus Universitet | |||||||||||||
Full Title: Postoperative analgesia after elective hip surgery - effect of obturator nerve blockade | |||||||||||||
Medical condition: No specific medical condition is investigated. The objective of the trial is to investigate a method for postoperative analgesia after elective hip surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005599-33 | Sponsor Protocol Number: AMSC-BDT-001 | Start Date*: 2013-06-10 | |||||||||||
Sponsor Name:Lékařská fakulta Univerzity Karlovy v Hradci Králové | |||||||||||||
Full Title: Utilization of Autologous Multipotent Mesenchymal Stem Cells in the Management of the Large Skeletal Defects during Revision Total Hip Arthroplasty: a Prospective, Non-randomized, Open-Label Study ... | |||||||||||||
Medical condition: Revision total hip arthroplasty. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004501-12 | Sponsor Protocol Number: 001-2013 | Start Date*: 2013-12-20 | ||||||||||||||||
Sponsor Name:Departement of Anesthesiology, Næstved Hospital | ||||||||||||||||||
Full Title: Effect of a lateral nerve of the thigh block on postoperative pain after total hip replacement surgery: a clinical radomised trial. | ||||||||||||||||||
Medical condition: Pain after total hip replacement surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004906-12 | Sponsor Protocol Number: ASK-3-2011 | Start Date*: 2011-11-07 | |||||||||||
Sponsor Name:Erling Bjerregaard Pedersen, Medicinsk forskningsafsnit, Regionshospitalet Holstebro | |||||||||||||
Full Title: Effect of hydroxyethyl starch on renal handling of sodium and water, vasoactive hormones,biomarkers and the circulatory system in patients undergoing hip replacement surgery | |||||||||||||
Medical condition: Patients undergoing hip replacement in spinal anesthesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000791-15 | Sponsor Protocol Number: 1308015 | Start Date*: 2013-08-08 | |||||||||||
Sponsor Name:CHU de Saint-Etienne | |||||||||||||
Full Title: Evaluation of postoperative administration of tranexamic acid on reducing blood loss after hip prothesis surgery. | |||||||||||||
Medical condition: surgery for hip prosthesis or for hip prosthesis replacement | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004955-38 | Sponsor Protocol Number: NL38327.018.11 | Start Date*: 2011-12-16 | ||||||||||||||||
Sponsor Name:AMC, Amsterdam | ||||||||||||||||||
Full Title: Controlling Glucose during Elective hip Surgery to study the influence on Coagulation | ||||||||||||||||||
Medical condition: patients who will undergo elective hip surgery with a hyperglycemic period perioperatively due to surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002239-16 | Sponsor Protocol Number: SM2-KHT-2015 | Start Date*: 2015-08-12 | ||||||||||||||||
Sponsor Name:Næstved Hospital | ||||||||||||||||||
Full Title: PANSAID – PAracetamol and NSAID in combination: A randomised, blinded, parallel 4-group clinical trial | ||||||||||||||||||
Medical condition: Pain after total hip replacement surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-001725-25 | Sponsor Protocol Number: RSA-HIP220306 | Start Date*: 2007-08-09 | |||||||||||
Sponsor Name:GREATER GLASGOW HEALTH BOARD | |||||||||||||
Full Title: REVISION HP REPLACEMENT - ACETABULAR IMPACTION GRAFTING - A RADIOSTEREOMETRIC COMPARISON BETWEEN FRESH FROZEN ALLOGRAFT AND MARROW-DEPLETED BONE WITH CALCIUM PHOSPHATE PLUS OR MINUS BONE MORPHOGENI... | |||||||||||||
Medical condition: REVISION HIP REPLACEMENT | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001791-13 | Sponsor Protocol Number: OXY4009 | Start Date*: 2005-08-31 | |||||||||||
Sponsor Name:Mundipharma GmbH | |||||||||||||
Full Title: An open-label, randomized, parallel-group, monocenter study to evaluate safety and efficacy of Oxycodone Hydrochloride administered orally (CR) and intravenously in patients with total hip endopros... | |||||||||||||
Medical condition: Male and female patients who are designated for a total hip endoprosthesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002746-35 | Sponsor Protocol Number: D4003C00030 | Start Date*: 2005-07-13 |
Sponsor Name:AstraZeneca AB | ||
Full Title: The "EXTEND" study: A randomized, double-blind, parallel-group, phase IIIb, multi-centre study evaluating extended prophylactic treatment with melagatran/ximelagatran versus enoxaparin for the prev... | ||
Medical condition: Prophylactic treatment for the prevention of venous thromboembolic events in patients undergoing elective hip replacement or hip fracture surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) SE (Completed) HU (Completed) AT (Completed) DK (Completed) DE (Completed) PT (Prematurely Ended) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001580-30 | Sponsor Protocol Number: 2006.SUR.ORT.01 | Start Date*: 2006-10-13 |
Sponsor Name:Royal Cornwall Hospitals NHS Trust | ||
Full Title: Investigation into the effects of steroid and local anaesthetic infiltration into soft tissues in total hip replacement wounds on post-operative pain relief. | ||
Medical condition: patients undergoing total hip replacement surgery for osteoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002457-41 | Sponsor Protocol Number: 150-CL-008 | Start Date*: 2006-05-15 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: Direct Factor Xa inhibitor YM150 for prevention of venous thromboembolism in patients undergoing elective total hip replacement. A double blind, parallel, dose-finding study in comparison with open... | |||||||||||||
Medical condition: Elective primary hip replacement surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) CZ (Completed) SK (Completed) DE (Completed) SE (Completed) NO (Completed) FI (Completed) PT (Completed) GR (Completed) IT (Completed) LT (Completed) EE (Prematurely Ended) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004445-42 | Sponsor Protocol Number: 1 | Start Date*: 2007-05-22 |
Sponsor Name:Institut for Pharmacology and Toxicology | ||
Full Title: Pharmacokinetics of Cetriaxon in bone | ||
Medical condition: hip replacement | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003898-42 | Sponsor Protocol Number: 2 | Start Date*: 2008-03-19 |
Sponsor Name:Institut for Pharmacology and Toxicology | ||
Full Title: Pharmacokinetica of levofloxacine in bone | ||
Medical condition: hip or knee replacement | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
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