- Trials with a EudraCT protocol (628)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (40)
628 result(s) found for: Knee.
Displaying page 1 of 32.
EudraCT Number: 2009-012043-42 | Sponsor Protocol Number: RSCH 01/10 | Start Date*: 2011-07-11 | ||||||||||||||||
Sponsor Name:Royal Surrey County Hospital NHS Trust | ||||||||||||||||||
Full Title: The Effect of a Human Surgical Sealant on Range of Motion in Total Knee Replacement | ||||||||||||||||||
Medical condition: Use of human surgical sealant during total knee replacement and if this affects knee movement for the 1st year after surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002635-23 | Sponsor Protocol Number: NBF_HK_02_2018. | Start Date*: 2018-10-23 | ||||||||||||||||||||||||||
Sponsor Name:Anaesthesia Department, Hvidovre Hospital, Capital Region of Denmark. | ||||||||||||||||||||||||||||
Full Title: Highdose steroids in High Pain Responders undergoing total knee-arthroplasty - A randomized doubleblindet controlled trial. | ||||||||||||||||||||||||||||
Medical condition: Perioperative management of a group of High Pain Responders in total knee-arthroplasty because of kneeosteoarthritis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002170-39 | Sponsor Protocol Number: Knemo01 | Start Date*: 2017-09-14 | |||||||||||
Sponsor Name:Eksote | |||||||||||||
Full Title: Combination of intrathecal morphine and local infiltration analgesia in treatment postoperative pain of total knee arthroplasty | |||||||||||||
Medical condition: Postoperative pain after total knee arthroplasty | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003169-33 | Sponsor Protocol Number: 2013-578 | Start Date*: 2013-10-30 | |||||||||||
Sponsor Name:Anders Troelsen | |||||||||||||
Full Title: Evaluation of intra articular Tranexamic acid for reduction of total blood loss in total knee unilateral arthroplasty | |||||||||||||
Medical condition: The benefit of additional Tranexamic Acid (TXA) injected intra-articular at the end of surgery for patients undergoing a unilateral total knee arthroplasty in addition to conventional IV TXA to red... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003513-40 | Sponsor Protocol Number: Bupi-Cata-TYKS-version 1.0. | Start Date*: 2006-08-21 | |||||||||||
Sponsor Name:Kalevi Pihlajamäki | |||||||||||||
Full Title: Intrathecal bupivacaine and clonidine for ambulatory knee arthroscopy | |||||||||||||
Medical condition: Patients are submitted for ambulatory knee arthroscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003756-37 | Sponsor Protocol Number: ANT-005 | Start Date*: 2020-02-25 | |||||||||||
Sponsor Name:Anthos Therapeutics | |||||||||||||
Full Title: A Multicenter, Randomized, Open-Label, Blinded Endpoint Evaluation, Active-Controlled, Dose-Ranging Study to Compare the Efficacy and Safety of i.v. MAA868 and s.c. Enoxaparin in Adult Patients Und... | |||||||||||||
Medical condition: Elective unilateral total knee arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) BE (Completed) LV (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000126-39 | Sponsor Protocol Number: 07-127 | Start Date*: 2008-05-26 | |||||||||||
Sponsor Name:CHU de Caen | |||||||||||||
Full Title: Analgésie post-opératoire pour prothèse totale de genou par cathéter péri-nerveux fémoral: Etude comparative de la levobupivacaine 0,125% versus ropivacaine 0, 2%. Protocole LPTG | |||||||||||||
Medical condition: Prothèse totale du genou | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003051-37 | Sponsor Protocol Number: 2013-07-03 | Start Date*: 2013-08-28 | ||||||||||||||||
Sponsor Name:Kuopion yliopistollinen sairaala | ||||||||||||||||||
Full Title: | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001214-10 | Sponsor Protocol Number: AAUH-01-2015 | Start Date*: 2015-06-02 | ||||||||||||||||
Sponsor Name:Aalborg universitets hospital [...] | ||||||||||||||||||
Full Title: Analgetic effect of perioperative klorzoxazon at total hip or knee arthroplasty | ||||||||||||||||||
Medical condition: Perioperative pain after incertion of hip or knee arthroplasty | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001906-41 | Sponsor Protocol Number: MRHT_ES-IF_RCT001 | Start Date*: 2016-08-08 | |||||||||||
Sponsor Name:Royal College of Surgeons in Ireland | |||||||||||||
Full Title: A randomised control trial of intra articular injectates in knee osteoarthritis: A comparison of corticosteroid (Methylprednisolone Acetate) and NSAID (Ketorolac tromethamine) injections | |||||||||||||
Medical condition: Knee osteoarthritis is the condition of interest. Osteoarthritis is a common musculoskeletal complaint, with an underlying pathogenesis related to bio-mechanical stress loading, resulting in initia... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001099-39 | Sponsor Protocol Number: SM1-KAKG-2018 | Start Date*: 2018-06-08 | ||||||||||||||||
Sponsor Name:Naestved Hospital | ||||||||||||||||||
Full Title: Dexamethasone twice for pain treatment of total knee arthroplasty (DEX-2-TKA) A randomized blinded placebo-controlled clinical trial | ||||||||||||||||||
Medical condition: Postoperative pain after total knee arthroplasty | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-015849-22 | Sponsor Protocol Number: 2009/147 | Start Date*: 2010-01-27 | |||||||||||
Sponsor Name:Salford Royal Foundation NHS Trust | |||||||||||||
Full Title: An open label study of intra-articular steroid injection in the management of symptomatic knee OA | |||||||||||||
Medical condition: Osteoarthritis of the Knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001151-19 | Sponsor Protocol Number: DKOA21 | Start Date*: 2007-08-21 | |||||||||||
Sponsor Name:Sint Maartenskliniek | |||||||||||||
Full Title: Placebo controlled trial to evaluate the effect on pain and function of six months treatment doxycycline in established knee osteoarthritis | |||||||||||||
Medical condition: Osteoarthritis of the knee, mild to severe pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005020-38 | Sponsor Protocol Number: KF7039-02 | Start Date*: 2022-07-12 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, Phase III trial to evaluate the efficacy and safety of a single intra-articular injection of RTX-GRT7039 in adult subjects with pain associated with ... | |||||||||||||
Medical condition: Moderate to severe pain associated with osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DK (Completed) PT (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-006110-20 | Sponsor Protocol Number: RepeatDoseTKAHPR2020 | Start Date*: 2021-06-18 | ||||||||||||||||
Sponsor Name:Vejle Sygehus, Ortopædkirurgisk afdeling, Forskningsenheden (COFU) | ||||||||||||||||||
Full Title: Repeat dose steroid to prevent pain relapse after Total Knee Arthroplasty in patients with high pain response - A randomized blinded placebo-controlled trial | ||||||||||||||||||
Medical condition: Periooperative management of total knee-arthroplasty because of knee-osteoarthritis. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000754-35 | Sponsor Protocol Number: R118528 | Start Date*: 2017-07-18 | |||||||||||
Sponsor Name:The University of Manchester | |||||||||||||
Full Title: The effect of Denosumab on Pain and bone Marrow Lesions in symptomatic Knee Osteo-arthritis: A Randomised Double Blind Placebo controlled Clinical Trial | |||||||||||||
Medical condition: Knee osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000444-26 | Sponsor Protocol Number: TM-CS+SG/301 | Start Date*: 2013-05-24 | |||||||||||
Sponsor Name:Tedec-Meiji Farma, S.A. | |||||||||||||
Full Title: Phase III clinical trial to evaluate the efficacy and safety of chondroitin sulphate and glucosamine sulphate in combination versus placebo in patients with osteoarthritis of the knee. | |||||||||||||
Medical condition: Knee osteoarthritis. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003795-39 | Sponsor Protocol Number: TKADEX | Start Date*: 2020-12-15 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Premedication with intranasal dexmedetomidine in sedation of patients undergoing total knee arthroplasty (TKADEX) - a prospective, double blinded randomized controlled trial | |||||||||||||
Medical condition: Knee arthrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005029-26 | Sponsor Protocol Number: KF7039-01 | Start Date*: 2022-08-08 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, Phase III trial to evaluate the efficacy and safety of intra-articular injections of RTX-GRT7039 in adult subjects with pain associated with osteoart... | |||||||||||||
Medical condition: Moderate to severe pain associated with osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) NL (Completed) CZ (Completed) IT (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003124-33 | Sponsor Protocol Number: SPA-S-899-01-21 | Start Date*: 2023-05-15 | |||||||||||
Sponsor Name:SPA-SOCIETÀ PRODOTTI ANTIBIOTICI S.P.A. | |||||||||||||
Full Title: Adaptative, multicenter, randomized, double-blind, parallel-group, placebo controlled, clinical trial, on the efficacy and tolerability of different escalating doses of intra-articular clodronate i... | |||||||||||||
Medical condition: Patients with painful knee osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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