- Trials with a EudraCT protocol (42)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
42 result(s) found for: Hip prosthesis.
Displaying page 1 of 3.
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 | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001906-41 | Sponsor Protocol Number: CHUBX2019/24 | Start Date*: 2021-06-16 |
Sponsor Name:CHU DE BORDEAUX | ||
Full Title: Benefit of positons emission tomography / 68Gallium citrate tomodensitometry for artificial hip and knee chronic infection diagnosis | ||
Medical condition: joint prosthesis infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
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. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002557-68 | Sponsor Protocol Number: CDJN608 FI01 | Start Date*: 2006-11-06 |
Sponsor Name:Hospital District of Southwest Finland | ||
Full Title: A randomized, double-blind, placebo-controlled study to evaluate the efficacy of zoledronic acid in enhancement of early stability of cementless primary hip prosthesis | ||
Medical condition: Bone loss occurring around cementless hip prosthesis in postmenopausal women treated for primary hip osteoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FI (Completed) | ||
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: | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014414-98 | Sponsor Protocol Number: 58185 | Start Date*: 2009-10-29 |
Sponsor Name:Department of Orthopaedic Surgery University Hospital Linköping | ||
Full Title: The impact of local bisphosphonate treatment on prosthetic fixation | ||
Medical condition: Osteoarthritis of the hip joint treated with total hip replacement | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
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 | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (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. | |||||||||||||
|
|||||||||||||
Population Age: Adults | 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... | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001655-72 | Sponsor Protocol Number: 69HCL15_0189 | Start Date*: 2015-07-13 | ||||||||||||||||
Sponsor Name:Hospices Civils de Lyon | ||||||||||||||||||
Full Title: Analgésie postopératoire par infiltration locale peropératoire versus blocs fémoral et cutané latéral de la cuisse dans la chirurgie de prothèse totale de hanche | ||||||||||||||||||
Medical condition: Douleur liée à la prothèse totale de hanche | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-004192-16 | Sponsor Protocol Number: 3.0 | Start Date*: 2023-04-12 | ||||||||||||||||
Sponsor Name:idival | ||||||||||||||||||
Full Title: Evaluation of the efficacy of treatment with mucosal bacterial vaccines (autovaccines) versus suppressive antibiotic treatment in subjects with hip or knee prosthesis infections. | ||||||||||||||||||
Medical condition: Patients with chronic infections of hip and knee prostheses, without the possibility of curative treatment of the infection. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004552-37 | Sponsor Protocol Number: 18CH052 | Start Date*: 2019-05-07 | |||||||||||
Sponsor Name:CHU SAINT-ETIENNE | |||||||||||||
Full Title: Dose Study of Tranexamic Acid in Total Hip Replacement to Reduce Postoperative Hemoglobin Loss. A Phase 2 Randomized Double-blind Monocentric Study | |||||||||||||
Medical condition: Arthropathy of Hip | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002965-19 | Sponsor Protocol Number: 1 | Start Date*: 2005-03-14 |
Sponsor Name:Orthopaedic department, Karolinska Institutet, Danderyd's Hospital | ||
Full Title: Can risedronate prevent periprosthetic bone loss after hip arthroplasty? A randomized, double-blind, placebo-controlled trial | ||
Medical condition: Periprosthetic bone loss after total hip arthroplasty (THA) is the main factor in limiting the longevity of implants used för treatment of osteoarthritis. Bone loss leads to implant destabilization... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
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 | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000541-20 | Sponsor Protocol Number: STH15714 | Start Date*: 2011-09-20 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Effect of Denosumab on Osteolytic Lesion Activity in Total Hip Arthroplasty (THA) | |||||||||||||
Medical condition: Prosthesis-related osteolysis after total hip arthroplasty | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
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 | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
