- 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 5 of 6.
EudraCT Number: 2009-015799-92 | Sponsor Protocol Number: FER-SURG02-Pilot | Start Date*: 2009-12-02 |
Sponsor Name:Universitätspital Zürich Anästhesie | ||
Full Title: Intravenous ferric carboxymaltose (Ferinject®) with or without Erythropoietin for the correction of preoperative anaemia in patients undergoing orthopaedic surgery | ||
Medical condition: • To evaluate the effect of the administration of ferric carboxymaltose (Ferinject®) with or without erythropoietin vs. no treatment (standard therapy) on the preoperative anaemia status in patient... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000698-30 | Sponsor Protocol Number: LK10 | Start Date*: 2011-04-18 | |||||||||||
Sponsor Name:Henrik Kehlet | |||||||||||||
Full Title: Postoperative søvnforstyrrelser efter Zolpidem behandling ved fast-track hofte- eller knæalloplastik | |||||||||||||
Medical condition: Postoperative REM sleep reduction after fast-track hip and knee arthroplasty. Comparison of preoperative level and level of REM on first postoperative night. The effect of one administration of Zo... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004285-15 | Sponsor Protocol Number: SM2-PJ-11 | Start Date*: 2011-09-22 | |||||||||||
Sponsor Name:Professor Jørgen Berg Dahl | |||||||||||||
Full Title: A comparison of the efficacy of the Adductor-Canal-Blockade vs. the femoral nerve block on muscle strength and mobilization in healthy volunteers: a randomized study | |||||||||||||
Medical condition: Healthy volunteers (intended for postoperative pain treatment in patients after total knee arthroplasty) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002280-18 | Sponsor Protocol Number: FIPRA#3 | Start Date*: 2017-09-18 | |||||||||||
Sponsor Name:Nordsjællands Hospital Hillerød | |||||||||||||
Full Title: Catheter-based peripheral regional anaesthesia after orthopaedic surgery: Comparison of low dose, automated periodic infusions with conventional high dose, continuous infusion, and patient-initiat... | |||||||||||||
Medical condition: Postoperative pain, after orthopaedic surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002925-39 | Sponsor Protocol Number: CMAA868A2201 | Start Date*: 2018-02-23 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A multicenter, randomized, open-label, blinded endpoint evaluation, active-controlled Phase 2 study to compare the efficacy and safety of s.c. MAA868 versus s.c. enoxaparin in adult patients underg... | |||||||||||||
Medical condition: venous thromboembolism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) AT (Prematurely Ended) CZ (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002465-18 | Sponsor Protocol Number: PROTEDI | Start Date*: 2019-12-16 |
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||
Full Title: Efficacy and tolerance of 4 weeks of tedizolid in prosthetic joint infections treated with implant removal | ||
Medical condition: prosthetic joint infections treated with implant removal. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004469-11 | Sponsor Protocol Number: PP-SA-001 | Start Date*: 2022-01-11 |
Sponsor Name:PHERECYDES PHARMA | ||
Full Title: PhagoDAIR I: A Phase I/II Multicenter, Randomized, Double-Blind Study to Evaluate Efficacy and Safety of Phage Therapy in Patients with Hip or Knee Prosthetic Joint Infection due to Staphylococcus ... | ||
Medical condition: knee or hip prosthetic joint infection (PJI) due to Staphylococcus aureus, with the indication of DAIR and Suppressive Antibiotics Therapy (SAT | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-018182-13 | Sponsor Protocol Number: 671975 | Start Date*: 2010-04-14 | |||||||||||
Sponsor Name:Ainara Aguirre Caballero | |||||||||||||
Full Title: Efectividad del magnesio epidural para reducir las necesidades de analgesia postoperatoria | |||||||||||||
Medical condition: Reducción del consumo de opiaceos y anestésicos locales por vía epidural tras cirugía de prótesis total de rodilla. Reduction of consumption of epidural opioid and local anesthetic drugs after tota... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000663-45 | Sponsor Protocol Number: PREVENT-iT-2021.07 | Start Date*: 2023-02-01 |
Sponsor Name:Hamilton Health Sciences Corporation | ||
Full Title: Prospective Randomized Evaluation of Emerging Novel Treatments for Infection prophylaxis in Total Joint Replacement (PREVENT-iT): A Pilot Study | ||
Medical condition: Persistent Draining Wound and Periprosthetic Joint Infection prevention in patients undergoing total joint replacement | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004601-32 | Sponsor Protocol Number: SM4-UG-14 | Start Date*: 2015-01-07 | |||||||||||
Sponsor Name:Gentofte Hospital | |||||||||||||
Full Title: The Effect of Local Anesthetic Volume within the Adductor Canal on Quadriceps Function Evaluated by Electromyography: A Randomized, Observer-Masked, Placebo-Controlled Study in Volunteers. | |||||||||||||
Medical condition: Healthy volunteers. Results will be used for optimizing the treatment of post-operative pain after total knee arthroplasty | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006699-40 | Sponsor Protocol Number: PTR2007 | Start Date*: 2008-03-03 | |||||||||||
Sponsor Name:Hospital Clínic | |||||||||||||
Full Title: Estudio aleatorizado y doble ciego para establecer el momento más apropiado de la administración de la profilaxis antibiótica en la artroplastia total de rodilla cuando se realiza bajo isquemia Ran... | |||||||||||||
Medical condition: Prevention of infection after total knee arthroplasty Prevención de la infección tras artroplastia total de rodilla | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004986-15 | Sponsor Protocol Number: Protocol_AFCN_17022019 | Start Date*: 2019-02-18 | |||||||||||||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
Full Title: Ultrasound-guided nerve block of the anterior femoral cutaneous nerves in healthy volunteers | |||||||||||||||||||||||
Medical condition: Pain around the surgical incision after total knee arthroplasty (TKA). The area anesthetized by a combination of nerve block techniques anesthetizing the anterior femoral cutaneous nerves are inve... | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-003688-30 | Sponsor Protocol Number: CS I-040101/02 | Start Date*: 2007-02-27 | |||||||||||
Sponsor Name:Kuros Biosurgery AG | |||||||||||||
Full Title: A phase 2 randomized, controlled, open-label (dose-blinded), multi-center, dose-finding study of the safety and efficacy of I-0401 in the treatment of patients with fractures of the tibial plateau ... | |||||||||||||
Medical condition: Fractures of the tibial plateau requiring grafting | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) IT (Completed) FR (Completed) HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002955-40 | Sponsor Protocol Number: 69HCL20_0111 | Start Date*: 2020-08-12 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Postoperative analgesic effect of orally administrated nefopam after a total knee arthroplasty: a randomized controlled trial | |||||||||||||
Medical condition: Major patients who have a surgery in the orthopedic surgery department of the Croix Rousse hospital for a total knee replacement. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2023-000172-36 | Sponsor Protocol Number: CHUB-Methadone | Start Date*: 2023-02-28 | |||||||||||
Sponsor Name:CHU Brugmann | |||||||||||||
Full Title: Intraoperative methadone for the prevention of postoperative pain: a randomized, double-blind clinical study in orthopedic surgery. | |||||||||||||
Medical condition: Orthopedic surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003078-41 | Sponsor Protocol Number: MUC-2/16 | Start Date*: 2018-11-23 |
Sponsor Name:MUCOS Pharma CZ s.r.o. | ||
Full Title: Reduction of post-traumatic systemic inflammatory response by Phlogenzym® using total hip replacement as a model. | ||
Medical condition: Total hip replacement | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-005115-26 | Sponsor Protocol Number: SKY0402-C-208 | Start Date*: 2008-01-21 |
Sponsor Name:Pacira Pharmaceuticals Inc. | ||
Full Title: A Multicenter, Randomized, Double-Blind, Parallel-Group, Active-Control, Dose-Ranging Study to Evaluate the Safety, Efficacy, and Comparative Systemic Bioavailability of a Single Administration of ... | ||
Medical condition: post-operative pain management | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) AT (Prematurely Ended) DE (Completed) DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-004942-12 | Sponsor Protocol Number: Protokol_MFCN_10102020 | Start Date*: 2020-11-19 | |||||||||||||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
Full Title: Selective ultrasound-guided nerve block of the medial femoral cutaneous nerve in healthy volunteers | |||||||||||||||||||||||
Medical condition: Pain around the surgical incisions after total knee arthroplasty (TKA). The area anesthetized by new nerve block techniques anesthetizing the medial femoral cutaneous nerve are investigated in heal... | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002670-36 | Sponsor Protocol Number: OXN3503 | Start Date*: 2009-01-30 | ||||||||||||||||
Sponsor Name:Mundipharma Research GmbH & Co. KG | ||||||||||||||||||
Full Title: A randomised, double-blind, double-dummy, parallel-group multicentre study to demonstrate non-inferiority in pain and locomotor function and improvement in symptoms of constipation in subjects with... | ||||||||||||||||||
Medical condition: Pain, locomotor function and improvement in constipation in osteoarthritis patients taking opioids | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) CZ (Completed) HU (Completed) NL (Completed) ES (Completed) AT (Completed) FI (Completed) BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-018173-31 | Sponsor Protocol Number: POISE-2 | Start Date*: 2011-02-25 | |||||||||||
Sponsor Name:Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau | |||||||||||||
Full Title: Ensayo clínico factorial de clonidina y aspirina en pacientes que van a ser sometidos a cirugía no cardiaca y que estén en riesgo moderado o alto de sufrir eventos cardíacos perioperatorios (Estudi... | |||||||||||||
Medical condition: Prevención de episodios cardiovasculares en pacientes de moderado a alto riesgo cardiovascular que son sometidos a una cirugía no cardiaca. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) AT (Completed) BE (Completed) DK (Completed) GB (Completed) DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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