- Trials with a EudraCT protocol (176)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
176 result(s) found for: Arthroplasty.
Displaying page 1 of 9.
| 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: View results | ||||||||||||||||||
| EudraCT Number: 2021-001708-14 | Sponsor Protocol Number: ABOGRAFT-01 | Start Date*: 2021-06-29 |
| Sponsor Name:Region Östergötland | ||
| Full Title: Antibiotic Impregnated Bone Graft to reduce infection in hip replacement. The ABOGRAFT trial | ||
| Medical condition: Patients scheduled for any type of hip arthroplasty requiring bone grafting | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-006930-17 | Sponsor Protocol Number: 01/2006 | Start Date*: 2007-03-20 | ||||||||||||||||
| Sponsor Name:HOSPITAL GENERAL DE VIC | ||||||||||||||||||
| Full Title: ANESTESIA SUBARACNOIDEA SELECTIVA. COMPARACIÓN DE BUPIVACAINA HIPERBÁRICA CON PRILOCAINA HIPERBÁRICA PARA ARTROSCOPIA DE RODILLA O HERNIOPLASTIA INGUINAL EN CIRUGIA MAYOR AMBULATORIA | ||||||||||||||||||
| Medical condition: Pacientes que se sometan a una artroplastia de rodilla ya sea diagnóstica o terapéutica y pacientes que se sometan a una hernioplastia inguinal | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-018245-21 | Sponsor Protocol Number: H-A-2009-069 | Start Date*: 2010-06-22 | |||||||||||
| Sponsor Name:Rigshospitalet | |||||||||||||
| Full Title: Fibrinklæber ved bilateral knæalloplastik – et prospektivt randomiseret studie med fokus på: blodtab, smerte, ROM, hævelse og styrke | |||||||||||||
| Medical condition: Formålet med nærværende studie er at undersøge om – og i bekræftende fald omfanget heraf – fibrinklæber (Evicel) reducerer blødningen efter Total Knæ Alloplastik (kunstigt knæ) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000692-14 | Sponsor Protocol Number: HKO-22112010 | Start Date*: 2011-11-03 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Hannu Kokki | ||||||||||||||||||||||||||||||||||||||
| 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: 2008-006528-67 | Sponsor Protocol Number: H-A-2008-030 | Start Date*: 2009-03-25 | |||||||||||
| Sponsor Name:Hvidovre Hospital, Anæstesiologisk afdeling 532 | |||||||||||||
| Full Title: Den perioperative effekt af methylprednisolon ved hoftealloplastik: et prospektivt, dobbeltblindet, placebokontrolleret studie. | |||||||||||||
| Medical condition: Total hip arthroplasty, postoperative pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2012-002889-12 | Sponsor Protocol Number: RH-4074-OJ2 | Start Date*: 2012-09-13 | ||||||||||||||||||||||||||
| Sponsor Name:Pär I Johansson | ||||||||||||||||||||||||||||
| Full Title: The effect of intraoperative low dose adrenaline on bleeding in total hip arthroplasty - a randomized placebo-controlled trial | ||||||||||||||||||||||||||||
| Medical condition: intra- and postoperative blood loss in total hip arthroplasty | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2018-002636-25 | Sponsor Protocol Number: NBF_HK_03_2018 | Start Date*: 2018-10-23 | |||||||||||||||||||||
| Sponsor Name:Anaesthesia Department, Hvidovre Hospital, Capital Region of Denmark. | |||||||||||||||||||||||
| Full Title: Highdose Steroid for High Pain Responders undergoing Total Hip-arthroplasty - A randomized doubleblindet controlled trial. | |||||||||||||||||||||||
| Medical condition: Perioperative management of total hip-arthroplasty because of hip-osteoarthritis | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2017-005180-40 | Sponsor Protocol Number: Protocol_PPB_TKA_31122017 | Start Date*: 2018-02-19 | |||||||||||||||||||||
| Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
| Full Title: The effect of the popliteal plexus block on postoperative pain after total knee arthroplasty - a randomized, controlled, double-blinded study | |||||||||||||||||||||||
| Medical condition: Postoperative posterior pain after total knee arthroplasty | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
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