- Trials with a EudraCT protocol (101)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
101 result(s) found for: Knee Arthroplasty.
Displaying page 2 of 6.
EudraCT Number: 2011-003556-39 | Sponsor Protocol Number: DARINA | Start Date*: 2012-06-05 |
Sponsor Name:Martini Hospital Groningen | ||
Full Title: A randomized pilot study comparing the safety of DAbigatran and RIvaroxaban versus NAdroparin in the prevention of venous thromboembolism after knee arthroplasty surgery. DARINA | ||
Medical condition: After total knee arthroplasty (TKA) surgery, patients are at risk to develop venous thromboembolism (VTE). Two novel agents, dabigatran and rivaroxaban, recently gained market authorisation for pre... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003408-21 | Sponsor Protocol Number: THO-IM_02-CT | Start Date*: 2015-12-09 | |||||||||||
Sponsor Name:Thrombotargets Europe | |||||||||||||
Full Title: A Phase II/III, randomized, controlled, single blind study to evaluate the haemostatic efficacy and safety of topically applied TT-173 in patients undergoing knee arthroplasty | |||||||||||||
Medical condition: Haemostatic effect in patients undergoing knee arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000180-32 | Sponsor Protocol Number: 761 | Start Date*: 2017-02-10 |
Sponsor Name:Sint Maartenskliniek Nijmegen | ||
Full Title: Pharmacokinetic Profile of Ropivacaine after Periarticular Local Infiltration Analgesia for Primary Total Knee Arthroplasty Without the use of a Tourniquet. | ||
Medical condition: patients receiving primary total knee replacement | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001836-72 | Sponsor Protocol Number: ISIS416858-CS3 | Start Date*: 2013-01-11 | |||||||||||
Sponsor Name:Isis Pharmaceuticals, Inc. | |||||||||||||
Full Title: An Open-label, Randomized, Active Comparator-Controlled, Adaptive Parallel-group Phase 2 Study to Assess the Safety and Efficacy of Multiple Doses of ISIS 416858 Administered Subcutaneously to Pati... | |||||||||||||
Medical condition: Prophylaxis of venous thromboembolism (VTE) in patients undergoing total knee arthroplasty (TKA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000694-22 | Sponsor Protocol Number: ACA-Germ-04-5 | Start Date*: 2005-11-17 |
Sponsor Name:Prof. Dr.Christian Werner | ||
Full Title: „Levobupivacaine for postoperative pain control in patients with knee arthroplasty – a comparison with ropivacaine“ | ||
Medical condition: patients undergoing total knee arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000071-24 | Sponsor Protocol Number: TRANEXTIME | Start Date*: 2016-03-10 |
Sponsor Name:Consorci Mar Parc de Salut de Barcelona (Parc de Salut MAR) | ||
Full Title: TIME OF ADMINISTRATION OF TRANEXAMIC ACID TO PREVENT BLEEDING IN TOTAL KNEE ARTHROPLASTY | ||
Medical condition: Total knee arthroplasty bleeding | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001232-59 | Sponsor Protocol Number: AGO/2019/002 | Start Date*: 2020-01-29 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: Safety and Efficacy of Patient Controlled Analgesia using the Sublingual Sufentanil Tablet System (SSTS) in a fast track rehabilitation program after Total Knee Arthroplasty. | |||||||||||||
Medical condition: Total Knee Arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001252-41 | Sponsor Protocol Number: NA | Start Date*: 2022-07-08 |
Sponsor Name:CHU de Liège | ||
Full Title: Preventing postoperative anaemia in total knee arthroplasty and impact of intravenous iron supplementation on postoperative functional recovery : a randomized clinical trial | ||
Medical condition: Total Knee Arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002438-35 | Sponsor Protocol Number: 860 | Start Date*: 2019-09-16 | ||||||||||||||||||||||||||
Sponsor Name:Radboudumc [...] | ||||||||||||||||||||||||||||
Full Title: Multiple doses versus single dose of cefazolin to prevent periprosthetic joint infection after revision arthroplasty: a multicenter open-label, randomized clinical trial. | ||||||||||||||||||||||||||||
Medical condition: Prevention of periprosthetic joint infection on patients undergoing revision surgery of the hip or knee. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003695-31 | Sponsor Protocol Number: FIB | Start Date*: 2017-12-04 | |||||||||||
Sponsor Name:Ziekenhuis Oost-Limburg | |||||||||||||
Full Title: Fascia iliaca block for analgesia in unilateral direct anterior approach total hip arthroplasty | |||||||||||||
Medical condition: Total hip arthroplasty through minimal invasive muscle sparing surgery technique | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002439-10 | Sponsor Protocol Number: PAKA-33601-AS117013 | Start Date*: 2013-10-23 | |||||||||||
Sponsor Name:University of Warwick [...] | |||||||||||||
Full Title: Perioperative Analgesia for Knee Arthroplasty: A prospective randomised controlled trial | |||||||||||||
Medical condition: Osteoarthritis of the knee is a common problem; it causes inability to walk without pain and a reduction in activity levels. Total knee replacements are performed for relief of this disabilitating ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001008-13 | Sponsor Protocol Number: 497 | Start Date*: 2013-09-18 |
Sponsor Name:Sint Maartenskliniek | ||
Full Title: Fast-track rehabilitation protocol for Total Knee Arthroplasty: A Randomized Controlled Trial comparing Local Infiltration Analgesia with Femoral Nerve Block | ||
Medical condition: patients requiring total knee arthroplasty for non-inflammatory osteoarthritis of the knee | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004046-15 | Sponsor Protocol Number: TKA4 | Start Date*: 2013-07-03 | |||||||||||
Sponsor Name:ORtopædkirurgisk Forskningsenhed, Aarhus Universitetshospital | |||||||||||||
Full Title: A 4-way randomized double-blinded migration (RSA), bone density (DXA), and biomarker study assessing adaptive bone changes and implant fixation and longevity of the new Regenerex Porous Titanium Ti... | |||||||||||||
Medical condition: Osteoarthritis in the knee treated with cementless total knee arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000082-23 | Sponsor Protocol Number: 2016-001-M | Start Date*: 2016-03-11 |
Sponsor Name:Reinier de Graaf Groep | ||
Full Title: Median Local Anaesthetic Dose (MLAD) of intrathecal Bupivacaine in total knee arthroplasty | ||
Medical condition: Spinal anaesthesia during total knee arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001618-13 | Sponsor Protocol Number: R475-OA-1816 | Start Date*: 2018-11-28 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: Study to Evaluate Arthroplasty Specimens in the Phase 3 Fasinumab Program for Osteoarthritis of the Knee and 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: GB (Prematurely Ended) PL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-000857-10 | Sponsor Protocol Number: NA | Start Date*: 2022-05-16 |
Sponsor Name:CHU de Liège | ||
Full Title: Isobaric versus hyperbaric intrathecal bupivacaine: influence of baricity on blood pression variation during elective total knee arthroplasty: a randomized clinical trial. | ||
Medical condition: Total knee arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022701-17 | Sponsor Protocol Number: 1709801154 | Start Date*: 2015-11-17 |
Sponsor Name:Isala | ||
Full Title: Reduction of surgical-site infection in hip and knee arthroplasty: the influence of perioperative mupirocin nasal ointment and chlorhexidine soap in a double-blind, randomized, multicentre, placebo... | ||
Medical condition: osteoarthritis of hip and knee, prevention of surgical site infections after arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011492-73 | Sponsor Protocol Number: 13.09 | Start Date*: 2009-09-28 |
Sponsor Name:Swindon and Marlborough NHS Foundation Trust | ||
Full Title: Analysis of Blood Loss With the Use of Fibrin Sealant in Total Knee Replacement Surgery – A Randomised Controlled Study | ||
Medical condition: Blood loss in total knee arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003010-93 | Sponsor Protocol Number: 620 | Start Date*: 2014-10-15 |
Sponsor Name:Sint Maartenskliniek | ||
Full Title: Pharmacokinetic Profile of Ropivacaïne after Periarticular Local Infiltration Analgesia for Primary Total Knee Arthroplasty | ||
Medical condition: patients receiving primary total knee replacement | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001808-37 | Sponsor Protocol Number: 612163 | Start Date*: 2006-09-13 |
Sponsor Name:Royal Devon and Exeter NHS Foundation Trust | ||
Full Title: A randomised controlled trial of fentanyl versus morphine following lower limb arthroplasty | ||
Medical condition: Patients with significant pain following hip or knee arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
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