- Trials with a EudraCT protocol (71)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
71 result(s) found for: Orthopedic surgery.
Displaying page 1 of 4.
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: 2013-001607-36 | Sponsor Protocol Number: 1 | Start Date*: 2013-08-23 |
Sponsor Name:SLL | ||
Full Title: Diagnosis of infection in prothesis by 18F-FDG-WBC-PET/CT | ||
Medical condition: orthopedic prothesis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-000941-11 | Sponsor Protocol Number: GMRA-102,Am.No.1 | Start Date*: 2013-03-27 |
Sponsor Name:Bracco Imaging S.p.A. | ||
Full Title: A PROSPECTIVE MULTICENTER COHORT STUDY EVALUATING THE LONG TERM RETENTION OF GADOLINIUM IN HUMAN BONE AND SKIN AFTER THE RETROSPECTIVE ADMINISTRATION OF MULTIHANCE® OR PROHANCE® IN COMPARISON WITH... | ||
Medical condition: Nephrogenic Systemic Fibrosis (NSF) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001134-33 | Sponsor Protocol Number: 012329 | Start Date*: 2019-06-18 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Does repeated administration of cefuroxime after orthopedic surgery provide a better prophylactic profile regarding postoperativ infection than a single administration of preoperative antimicrobia... | |||||||||||||
Medical condition: Orthopedic infections. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001138-17 | Sponsor Protocol Number: 240583 | Start Date*: 2013-07-11 | |||||||||||
Sponsor Name:Orthopedic Research in Aarhus | |||||||||||||
Full Title: In vivo measurement of cefuroxime in subcutaneous and bone tissue using microdialysis | |||||||||||||
Medical condition: Orthopedic infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003078-36 | Sponsor Protocol Number: 727258 | Start Date*: 2020-09-14 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: The RAS-study A reverse and anatomical prosthesis shoulder study Can we improve the prophylactic profile of antibiotic treatment in shoulder prosthesis surgery? - A clinical microdialysis study as... | |||||||||||||
Medical condition: Orthopedic infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002328-34 | Sponsor Protocol Number: KB056 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:KEDRION S.P.A | |||||||||||||
Full Title: Efficacy and safety evaluation of Kedrion Fibrin Sealant as an adjuvant for the control of hemostasis in pediatric patients undergoing abdominal or orthopedic surgery. Multicenter, randomized, cont... | |||||||||||||
Medical condition: Paediatric patients undergoing abdominal or orthopedic surgery | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004733-14 | Sponsor Protocol Number: GSKET102011 | Start Date*: 2012-03-22 |
Sponsor Name:Medizinische Universität Wien | ||
Full Title: Intravenous S-Ketamine as an Analgesic Adjunct to General Anesthesia in chronic opioid-tolerant patient | ||
Medical condition: In the present investigation, we will compare the perioperative subanesthetic infusion of ketamine with placebo in opioid-resistant patients undergoing major orthopedic surgery. By powering the stu... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-000217-21 | Sponsor Protocol Number: 310816 | Start Date*: 2018-03-22 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Do use of torniquete reduce the impact of the antibiotic treatment during orthopedic treatment? | |||||||||||||
Medical condition: Orthopedic infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002890-31 | Sponsor Protocol Number: Pregab1 | Start Date*: 2006-08-25 |
Sponsor Name:Dept. of Anaesthesia, Medical University of Vienna | ||
Full Title: Does Pregabalin reduce preoperative anxiety: a placebo controlled study | ||
Medical condition: Patients should receive Pregabalin or placebo as premedication one hour before ambulatory elective surgery. After this they have to assess their anxiety and pain with Visual Analog Scale (VAS) for ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001630-18 | Sponsor Protocol Number: CWL15001 | Start Date*: 2023-09-20 | |||||||||||
Sponsor Name:5med GmbH | |||||||||||||
Full Title: A randomized, parallel group, multi-center study of a fentanyl nasal spray compared with placebo nasal spray for postoperative pain management and prolonged open treatment over up to 120 hours post... | |||||||||||||
Medical condition: Management of pain following orthopedic surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) BG (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018600-87 | Sponsor Protocol Number: Peri-Trauma | Start Date*: 2010-02-24 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | |||||||||||||
Full Title: POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY: COMPARISON OF INTRAVENOUS ANALGESIA AND ONE-SHOT EPIDURAL LUMBAR NERVE BLOCK. | |||||||||||||
Medical condition: POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000258-12 | Sponsor Protocol Number: 230189 | Start Date*: 2014-10-15 | |||||||||||
Sponsor Name:Orthopedic Research in Aarhus | |||||||||||||
Full Title: Pharmacokinetics of vancomycin in cancellous and cortical bone obtained by microdialysis | |||||||||||||
Medical condition: Orthopedic infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005384-31 | Sponsor Protocol Number: RSIv80 | Start Date*: 2021-03-19 | ||||||||||||||||
Sponsor Name:Rigshospitalet | ||||||||||||||||||
Full Title: A single blinded multicenter randomized study comparing intubating conditions during rapid sequence induction with either suxamethonium 1.0 mg/kg or rocuronium 1.0 mg/kg in elderly patients (≥ 80 y... | ||||||||||||||||||
Medical condition: The aim of this study is to determine the proportion of excellent tracheal intubation conditions at 60 seconds after administration of either rocuronium 1.0 mg/kg or suxamethonium 1 mg/kg in patien... | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019216-20 | Sponsor Protocol Number: AZ2010 | Start Date*: 2010-05-01 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI CAGLIARI | |||||||||||||
Full Title: "Effects of drug treatment with bisphosphonates (zoledronic acid) in the prevention of skeletal events in breast cancer patients with osteoporosis. Significant correlation with some biological para... | |||||||||||||
Medical condition: Breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013481-10 | Sponsor Protocol Number: 437 | Start Date*: 2009-10-14 |
Sponsor Name:Sint Maartenskliniek | ||
Full Title: Pharmacokinetics of high dose Ropivacaine with and without epinephrine for combined femoral and sciatic nerve block in lower extremity surgery. A pilot study. | ||
Medical condition: combined femoral and sciatic nerve block for lower extremity orthopedic surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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: 2005-005697-71 | Sponsor Protocol Number: 060402 | Start Date*: 2006-01-26 | |||||||||||
Sponsor Name:Baxalta Innovations GmbH | |||||||||||||
Full Title: Antihemophilic Factor (Recombinant) Plasma/Albumin-Free Method (rAHF PFM): A Phase 3/4, Prospective, Controlled, Randomized, Multi-Center Study to Compare the Efficacy and Safety of Continuous Infu... | |||||||||||||
Medical condition: Subjects with Severe or Moderately Severe Hemophilia A (baseline factor VIII (FVIII) level <= 2% of normal) hemophilia A undergoing major orthopedic surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) SE (Completed) BE (Completed) PT (Completed) ES (Completed) HU (Completed) NL (Completed) GB (Completed) IT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000700-14 | Sponsor Protocol Number: 2 | Start Date*: 2019-07-08 |
Sponsor Name:Medical University Graz | ||
Full Title: Pilot-Study comparing analgosedation concepts during placement of regional anaesthesia with either fentanyl, remifentanil, clonidine, EMLA-Patch or placebo in regard of patient's wellbeing, pain an... | ||
Medical condition: Patient with elective orthopedic surgery that will be administered a regional anaesthesia will be subject of the investigation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000826-39 | Sponsor Protocol Number: S-20130165 | Start Date*: 2014-06-17 | |||||||||||
Sponsor Name:Ortopædkirurgisk afdeling Odense Universitetshospital | |||||||||||||
Full Title: Determining the tissue concentration of dicloxacillin using Microdialysis (on healthy male subjects) | |||||||||||||
Medical condition: The trial is conducted on healthy male volunteers. An intravenous dose of 2 grams of dicloxacillin is administered intravenously and the muscle- and subcutaneous tissue concentrations are measured ... | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: Removed from public view |
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