- Trials with a EudraCT protocol (282)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
282 result(s) found for: Knee joint.
Displaying page 1 of 15.
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
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. | ||||||||||||||||||
|
||||||||||||||||||
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 | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults | 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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) BE (Completed) LV (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000818-37 | Sponsor Protocol Number: MTX-071-P03 | Start Date*: 2018-06-28 | |||||||||||||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, single dose phase IIb exploratory study to document the clinical effects and safety of intra-articular injections of Lopain (MTX-071) in patients wit... | |||||||||||||||||||||||
Medical condition: chronic osteoarthritic knee joint pain | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) SK (Completed) HR (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 | |||||||||||||
|
|||||||||||||
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: | ||||||||||||||||||
|
||||||||||||||||||
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 | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001981-24 | Sponsor Protocol Number: MTX-071-P01 | Start Date*: 2016-02-04 | |||||||||||||||||||||
Sponsor Name:Mestex | |||||||||||||||||||||||
Full Title: Lopain (MTX-071 / resiniferatoxin) An open label, dose-escalating phase I/IIa study to determine the safety and clinical effects of intra-articular injections of Lopain (MTX-071) in patients wi... | |||||||||||||||||||||||
Medical condition: Chronic osteoarthritic knee-joint pain | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-003379-28 | Sponsor Protocol Number: 0663-098 | Start Date*: 2009-03-11 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III Randomized, Double-Blind, Placebo- and Active-Comparator-Controlled, Multiple-Dose, Clinical Trial to Study the Safety and Efficacy of MK-0663/Etoricoxib and Ibuprofen in the Treatment ... | |||||||||||||
Medical condition: Pain after total knee replacement | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) LT (Completed) EE (Completed) HU (Completed) SI (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003230-26 | Sponsor Protocol Number: MIV-711-201 | Start Date*: 2016-03-23 | |||||||||||
Sponsor Name:Medivir AB | |||||||||||||
Full Title: A Randomised, Double-blind Placebo-controlled Phase IIa Study to Evaluate Efficacy, Safety and Tolerability of MIV-711 in Knee Joint Osteoarthritis | |||||||||||||
Medical condition: Knee Joint Osteoarthritis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
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 | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001411-71 | Sponsor Protocol Number: R475-OA-1815 | Start Date*: 2018-12-03 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: Study to Evaluate Synovial Fluid in the Phase 3 Fasinumab Program for Osteoarthritis of the Knee and Hip | |||||||||||||
Medical condition: Pain due to osteoarthritis of the knee | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001970-33 | Sponsor Protocol Number: 167700-002CL | Start Date*: 2013-07-19 | |||||||||||
Sponsor Name:Proximagen Limited | |||||||||||||
Full Title: A Double-Blind, Randomised, Exploratory Study to Investigate the Safety, Efficacy and Pharmacokinetics of PRX167700 in Subjects with Knee Osteoarthritis. | |||||||||||||
Medical condition: Osteoarthritis of the knee | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-005000-17 | Sponsor Protocol Number: JU-BioMiStem-01 | Start Date*: 2021-09-20 | |||||||||||
Sponsor Name:Jagiellonian University | |||||||||||||
Full Title: A Randomized, Double Blind, Two Arms, Controlled Phase I/II Safety and Efficacy Study on MesoCellA-Ortho Tissue Engineered Product Intraarticularly Administrated in Adult Patients with Osteoarthrosis | |||||||||||||
Medical condition: articular knee diseases | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004087-30 | Sponsor Protocol Number: 1007612/30.04.2010 | Start Date*: 2011-08-25 | |||||||||||
Sponsor Name:Tartu University Department of Sports Medicine and Rehabilitation | |||||||||||||
Full Title: Effect of 12 weeks rehabilitation (aspect of neuromuscular physical therapy) in middle-aged patients in post-atroscopic period | |||||||||||||
Medical condition: Cartilage Lesion of the Knee Joint | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: EE (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 | |||||||||||||
|
|||||||||||||
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. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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. |
